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2020-10-24 06:01:02, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_004946               6117 bp    mRNA    linear   PRI 24-JUN-2013
DEFINITION  Homo sapiens dedicator of cytokinesis 2 (DOCK2), mRNA.
ACCESSION   NM_004946
VERSION     NM_004946.2  GI:205277317
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 6117)
  AUTHORS   Dulak,A.M., Stojanov,P., Peng,S., Lawrence,M.S., Fox,C.,
            Stewart,C., Bandla,S., Imamura,Y., Schumacher,S.E., Shefler,E.,
            McKenna,A., Carter,S.L., Cibulskis,K., Sivachenko,A., Saksena,G.,
            Voet,D., Ramos,A.H., Auclair,D., Thompson,K., Sougnez,C.,
            Onofrio,R.C., Guiducci,C., Beroukhim,R., Zhou,Z., Lin,L., Lin,J.,
            Reddy,R., Chang,A., Landrenau,R., Pennathur,A., Ogino,S.,
            Luketich,J.D., Golub,T.R., Gabriel,S.B., Lander,E.S., Beer,D.G.,
            Godfrey,T.E., Getz,G. and Bass,A.J.
  TITLE     Exome and whole-genome sequencing of esophageal adenocarcinoma
            identifies recurrent driver events and mutational complexity
  JOURNAL   Nat. Genet. 45 (5), 478-486 (2013)
   PUBMED   23525077
  REMARK    GeneRIF: DOCK2 mutations are associated with esophageal
            adenocarcinoma.
REFERENCE   2  (bases 1 to 6117)
  AUTHORS   Lauc,G., Huffman,J.E., Pucic,M., Zgaga,L., Adamczyk,B., Muzinic,A.,
            Novokmet,M., Polasek,O., Gornik,O., Kristic,J., Keser,T.,
            Vitart,V., Scheijen,B., Uh,H.W., Molokhia,M., Patrick,A.L.,
            McKeigue,P., Kolcic,I., Lukic,I.K., Swann,O., van Leeuwen,F.N.,
            Ruhaak,L.R., Houwing-Duistermaat,J.J., Slagboom,P.E., Beekman,M.,
            de Craen,A.J., Deelder,A.M., Zeng,Q., Wang,W., Hastie,N.D.,
            Gyllensten,U., Wilson,J.F., Wuhrer,M., Wright,A.F., Rudd,P.M.,
            Hayward,C., Aulchenko,Y., Campbell,H. and Rudan,I.
  TITLE     Loci associated with N-glycosylation of human immunoglobulin G show
            pleiotropy with autoimmune diseases and haematological cancers
  JOURNAL   PLoS Genet. 9 (1), E1003225 (2013)
   PUBMED   23382691
REFERENCE   3  (bases 1 to 6117)
  AUTHORS   Hanawa-Suetsugu,K., Kukimoto-Niino,M., Mishima-Tsumagari,C.,
            Akasaka,R., Ohsawa,N., Sekine,S., Ito,T., Tochio,N., Koshiba,S.,
            Kigawa,T., Terada,T., Shirouzu,M., Nishikimi,A., Uruno,T.,
            Katakai,T., Kinashi,T., Kohda,D., Fukui,Y. and Yokoyama,S.
  TITLE     Structural basis for mutual relief of the Rac guanine nucleotide
            exchange factor DOCK2 and its partner ELMO1 from their
            autoinhibited forms
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 109 (9), 3305-3310 (2012)
   PUBMED   22331897
  REMARK    GeneRIF: The C-terminal Pro-rich tail of ELMO1 winds around the
            Src-homology 3 domain of DOCK2 to form an intermolecular 5-helix
            bundle. The entire regions of both DOCK2 a& ELMO1 assemble to
            create a rigid structure required for the DOCK2 & ELMO1 binding.
REFERENCE   4  (bases 1 to 6117)
  AUTHORS   El-Haibi,C.P., Singh,R., Sharma,P.K., Singh,S. and Lillard,J.W. Jr.
  TITLE     CXCL13 mediates prostate cancer cell proliferation through JNK
            signalling and invasion through ERK activation
  JOURNAL   Cell Prolif. 44 (4), 311-319 (2011)
   PUBMED   21645150
  REMARK    GeneRIF: Our results show CXCL13-mediated PCa cell invasion
            requires Akt and ERK12 activation and suggests a new role for DOCK2
            in proliferation of hormone-refractory CXCR5-positive PCa cells.
REFERENCE   5  (bases 1 to 6117)
  AUTHORS   Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V.,
            Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S.
  CONSRTM   DREAM investigators
  TITLE     Variation at the NFATC2 locus increases the risk of
            thiazolidinedione-induced edema in the Diabetes REduction
            Assessment with ramipril and rosiglitazone Medication (DREAM) study
  JOURNAL   Diabetes Care 33 (10), 2250-2253 (2010)
   PUBMED   20628086
  REMARK    GeneRIF: Observational study of gene-disease association,
            gene-environment interaction, and pharmacogenomic / toxicogenomic.
            (HuGE Navigator)
REFERENCE   6  (bases 1 to 6117)
  AUTHORS   Nishihara,H., Maeda,M., Tsuda,M., Makino,Y., Sawa,H., Nagashima,K.
            and Tanaka,S.
  TITLE     DOCK2 mediates T cell receptor-induced activation of Rac2 and IL-2
            transcription
  JOURNAL   Biochem. Biophys. Res. Commun. 296 (3), 716-720 (2002)
   PUBMED   12176041
  REMARK    GeneRIF: DOCK2 mediates T cell receptor-induced activation of Rac2
            and IL-2 transcription in jurkat cells
REFERENCE   7  (bases 1 to 6117)
  AUTHORS   Reif,K. and Cyster,J.
  TITLE     The CDM protein DOCK2 in lymphocyte migration
  JOURNAL   Trends Cell Biol. 12 (8), 368-373 (2002)
   PUBMED   12191913
  REMARK    Review article
REFERENCE   8  (bases 1 to 6117)
  AUTHORS   Brugnera,E., Haney,L., Grimsley,C., Lu,M., Walk,S.F.,
            Tosello-Trampont,A.C., Macara,I.G., Madhani,H., Fink,G.R. and
            Ravichandran,K.S.
  TITLE     Unconventional Rac-GEF activity is mediated through the
            Dock180-ELMO complex
  JOURNAL   Nat. Cell Biol. 4 (8), 574-582 (2002)
   PUBMED   12134158
REFERENCE   9  (bases 1 to 6117)
  AUTHORS   Fukui,Y., Hashimoto,O., Sanui,T., Oono,T., Koga,H., Abe,M.,
            Inayoshi,A., Noda,M., Oike,M., Shirai,T. and Sasazuki,T.
  TITLE     Haematopoietic cell-specific CDM family protein DOCK2 is essential
            for lymphocyte migration
  JOURNAL   Nature 412 (6849), 826-831 (2001)
   PUBMED   11518968
REFERENCE   10 (bases 1 to 6117)
  AUTHORS   Nishihara,H., Kobayashi,S., Hashimoto,Y., Ohba,F., Mochizuki,N.,
            Kurata,T., Nagashima,K. and Matsuda,M.
  TITLE     Non-adherent cell-specific expression of DOCK2, a member of the
            human CDM-family proteins
  JOURNAL   Biochim. Biophys. Acta 1452 (2), 179-187 (1999)
   PUBMED   10559471
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            DB145764.1, BC104900.1, BC035613.1, BF110460.1 and BC084556.1.
            On Sep 19, 2008 this sequence version replaced gi:31377467.
            
            Summary: The protein encoded by this gene belongs to the CDM
            protein family. It is specifically expressed in hematopoietic
            cells, predominantly in the peripheral blood leukocytes, and is
            involved in remodeling of the actin cytoskeleton required for
            lymphocyte migration, through the activation of RAC. Mice lacking
            this gene show a severe impairment in the migration and homing of
            lymphocytes. These mutant mice also exhibited long-term survival of
            allografts, suggesting that this gene may be a target for
            controlling transplant rejection. [provided by RefSeq, Oct 2011].
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: D86964.1, BC104900.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025088 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-44                DB145764.1         1-44
            45-3274             BC104900.1         1-3230
            3275-3535           BC035613.1         916-1176
            3536-5649           BC104900.1         3492-5605
            5650-5854           BF110460.1         251-455
            5855-6117           BC084556.1         2136-2398
FEATURES             Location/Qualifiers
     source          1..6117
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="5"
                     /map="5q35.1"
     gene            1..6117
                     /gene="DOCK2"
                     /note="dedicator of cytokinesis 2"
                     /db_xref="GeneID:1794"
                     /db_xref="HGNC:2988"
                     /db_xref="HPRD:09121"
                     /db_xref="MIM:603122"
     exon            1..123
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    39..41
                     /gene="DOCK2"
                     /note="upstream in-frame stop codon"
     CDS             81..5573
                     /gene="DOCK2"
                     /note="dedicator of cyto-kinesis 2"
                     /codon_start=1
                     /product="dedicator of cytokinesis protein 2"
                     /protein_id="NP_004937.1"
                     /db_xref="GI:31377468"
                     /db_xref="CCDS:CCDS4371.1"
                     /db_xref="GeneID:1794"
                     /db_xref="HGNC:2988"
                     /db_xref="HPRD:09121"
                     /db_xref="MIM:603122"
                     /translation="
MAPWRKADKERHGVAIYNFQGSGAPQLSLQIGDVVRIQETCGDWYRGYLIKHKMLQGIFPKSFIHIKEVTVEKRRNTENIIPAEIPLAQEVTTTLWEWGSIWKQLYVASKKERFLQVQSMMYDLMEWRSQLLSGTLPKDELKELKQKVTSKIDYGNKILELDLIVRDEDGNILDPDNTSVISLFHAHEEATDKITERIKEEMSKDQPDYAMYSRISSSPTHSLYVFVRNFVCRIGEDAELFMSLYDPNKQTVISENYLVRWGSRGFPKEIEMLNNLKVVFTDLGNKDLNRDKIYLICQIVRVGKMDLKDTGAKKCTQGLRRPFGVAVMDITDIIKGKAESDEEKQHFIPFHPVTAENDFLHSLLGKVIASKGDSGGQGLWVTMKMLVGDIIQIRKDYPHLVDRTTVVARKLGFPEIIMPGDVRNDIYITLLQGDFDKYNKTTQRNVEVIMCVCAEDGKTLPNAICVGAGDKPMNEYRSVVYYQVKQPRWMETVKVAVPIEDMQRIHLRFMFRHRSSLESKDKGEKNFAMSYVKLMKEDGTTLHDGFHDLVVLKGDSKKMEDASAYLTLPSYRHHVENKGATLSRSSSSVGGLSVSSRDVFSISTLVCSTKLTQNVGLLGLLKWRMKPQLLQENLEKLKIVDGEEVVKFLQDTLDALFNIMMEHSQSDEYDILVFDALIYIIGLIADRKFQHFNTVLEAYIQQHFSATLAYKKLMTVLKTYLDTSSRGEQCEPILRTLKALEYVFKFIVRSRTLFSQLYEGKEQMEFEESMRRLFESINNLMKSQYKTTILLQVAALKYIPSVLHDVEMVFDAKLLSQLLYEFYTCIPPVKLQKQKVQSMNEIVQSNLFKKQECRDILLPVITKELKELLEQKDDMQHQVLERKYCVELLNSILEVLSYQDAAFTYHHIQEIMVQLLRTVNRTVITMGRDHILISHFVACMTAILNQMGDQHYSFYIETFQTSSELVDFLMETFIMFKDLIGKNVYPGDWMAMSMVQNRVFLRAINKFAETMNQKFLEHTNFEFQLWNNYFHLAVAFITQDSLQLEQFSHAKYNKILNKYGDMRRLIGFSIRDMWYKLGQNKICFIPGMVGPILEMTLIPEAELRKATIPIFFDMMLCEYQRSGDFKKFENEIILKLDHEVEGGRGDEQYMQLLESILMECAAEHPTIAKSVENFVNLVKGLLEKLLDYRGVMTDESKDNRMSCTVNLLNFYKDNNREEMYIRYLYKLRDLHLDCDNYTEAAYTLLLHTWLLKWSDEQCASQVMQTGQQHPQTHRQLKETLYETIIGYFDKGKMWEEAISLCKELAEQYEMEIFDYELLSQNLIQQAKFYESIMKILRPKPDYFAVGYYGQGFPSFLRNKVFIYRGKEYERREDFQMQLMTQFPNAEKMNTTSAPGDDVKNAPGQYIQCFTVQPVLDEHPRFKNKPVPDQIINFYKSNYVQRFHYSRPVRRGTVDPENEFASMWIERTSFVTAYKLPGILRWFEVVHMSQTTISPLENAIETMSTANEKILMMINQYQSDETLPINPLSMLLNGIVDPAVMGGFAKYEKAFFTEEYVRDHPEDQDKLTHLKDLIAWQIPFLGAGIKIHEKRVSDNLRPFHDRMEECFKNLKMKVEKEYGVREMPDFDDRRVGRPRSMLRSYRQMSIISLASMNSDCSTPSKPTSESFDLELASPKTPRVEQEEPISPGSTLPEVKLRRSKKRTKRSSVVFADEKAAAESDLKRLSRKHEFMSDTNLSEHAAIPLKASVLSQMSFASQSMPTIPALALSVAGIPGLDEANTSPRLSQTFLQLSDGDKKTLTRKKVNQFFKTMLASKSAEEGKQIPDSLSTDL
"
     misc_feature    114..281
                     /gene="DOCK2"
                     /note="Src Homology 3 domain of Class A Dedicator of
                     Cytokinesis protein 2; Region: SH3_DOCK2_A; cd12050"
                     /db_xref="CDD:212983"
     misc_feature    order(120..134,153..155,168..176,180..182,192..197,
                     207..212,216..218,240..242,246..248,252..254,258..260,
                     264..269,273..275,279..281)
                     /gene="DOCK2"
                     /note="ELMO interaction site [polypeptide binding]; other
                     site"
                     /db_xref="CDD:212983"
     misc_feature    order(129..131,135..137,144..146,156..158,207..212,
                     258..260,264..269)
                     /gene="DOCK2"
                     /note="peptide ligand binding site [polypeptide binding];
                     other site"
                     /db_xref="CDD:212983"
     misc_feature    705..707
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    714..716
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    990..992
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N6-acetyllysine; propagated from
                     UniProtKB/Swiss-Prot (Q92608.2); acetylation site"
     misc_feature    1344..1931
                     /gene="DOCK2"
                     /note="C2 domain; Region: C2; cl14603"
                     /db_xref="CDD:212363"
     misc_feature    1842..1844
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q92608.2); phosphorylation site"
     misc_feature    1857..1859
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q92608.2); phosphorylation site"
     misc_feature    2292..2294
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N6-acetyllysine; propagated from
                     UniProtKB/Swiss-Prot (Q92608.2); acetylation site"
     misc_feature    2895..4508
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q92608.2);
                     Region: Interaction with CRKL"
     misc_feature    3678..4940
                     /gene="DOCK2"
                     /note="Dock Homology Region 2, a GEF domain, of Class A
                     Dedicator of Cytokinesis 2; Region: DHR2_DOCK2; cd11706"
                     /db_xref="CDD:212579"
     misc_feature    order(3984..3986,4005..4013,4017..4019,4023..4028,
                     4032..4037,4044..4049,4053..4058,4065..4070,4077..4079,
                     4338..4340,4350..4361,4368..4370)
                     /gene="DOCK2"
                     /note="dimer interface [polypeptide binding]; other site"
                     /db_xref="CDD:212579"
     misc_feature    order(4182..4184,4188..4199,4245..4253,4302..4310,
                     4410..4421,4452..4457,4464..4466,4581..4583,4593..4595,
                     4653..4658,4662..4667,4677..4682,4689..4709,4716..4718,
                     4806..4808,4854..4856,4860..4865,4872..4874,4881..4883)
                     /gene="DOCK2"
                     /note="Rac binding site [polypeptide binding]; other site"
                     /db_xref="CDD:212579"
     misc_feature    4689..4706
                     /gene="DOCK2"
                     /note="nucleotide sensor; other site"
                     /db_xref="CDD:212579"
     misc_feature    5133..5135
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q92608.2); phosphorylation site"
     misc_feature    5142..5144
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    5145..5147
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    5196..5198
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    5271..5273
                     /gene="DOCK2"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q92608.2); phosphorylation site"
     variation       112
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200033547"
     exon            124..207
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       131
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185449432"
     variation       147
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376950305"
     variation       170
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:141894939"
     variation       173
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370494583"
     variation       179
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374789654"
     exon            208..248
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       214
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150182906"
     variation       228
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200852440"
     exon            249..304
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       301
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368156237"
     exon            305..401
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       311
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377614169"
     variation       318
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201979117"
     variation       320
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:185282572"
     variation       344
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201493926"
     variation       358
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138714263"
     variation       359
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144632263"
     variation       366
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370949354"
     exon            402..550
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       431
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112922689"
     variation       446
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35393134"
     variation       469
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:78450053"
     variation       479
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140206456"
     variation       485
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373741346"
     variation       542
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367573686"
     variation       550
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371312059"
     exon            551..686
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       587
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202075394"
     variation       599
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146530031"
     variation       600
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200805864"
     variation       617
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:143962640"
     variation       660
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147299638"
     exon            687..841
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       705
                     /gene="DOCK2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:148418103"
     variation       711
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151191554"
     variation       720
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150969388"
     variation       737
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:34039776"
     variation       747
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:370094182"
     variation       815
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374307327"
     variation       816
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139449745"
     variation       832
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78243868"
     variation       833
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146746458"
     variation       834
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140430355"
     exon            842..923
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       848
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:145405039"
     variation       890
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189140579"
     variation       908
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368563028"
     variation       914
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370245029"
     exon            924..1059
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       927
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369315365"
     variation       986
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146489287"
     variation       1028
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199921409"
     exon            1060..1135
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1072
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:149096712"
     variation       1097
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:375687811"
     variation       1103
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:368378335"
     variation       1114
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112557122"
     exon            1136..1212
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1142
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143288655"
     exon            1213..1338
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1226
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200816827"
     variation       1292
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:2112703"
     variation       1295
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141406325"
     exon            1339..1463
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1368
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370264550"
     variation       1373
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377517116"
     variation       1396
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113673055"
     variation       1414
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371303142"
     variation       1440
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114888195"
     variation       1441
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374175915"
     variation       1446
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368892236"
     variation       1454
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2306559"
     variation       1457
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144520292"
     exon            1464..1562
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1470
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372498181"
     variation       1476
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200560235"
     variation       1497
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201626676"
     variation       1515
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370114623"
     variation       1517
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147336443"
     variation       1529
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139876228"
     variation       1562
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:192453842"
     exon            1563..1635
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1566
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371391395"
     variation       1589
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369688871"
     variation       1626
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201439364"
     exon            1636..1739
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1674
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149411090"
     variation       1677
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375363462"
     variation       1680
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373197319"
     variation       1683
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143942535"
     variation       1709
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148641505"
     variation       1722
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143137802"
     exon            1740..1923
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1746
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199853621"
     variation       1748
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139368328"
     variation       1770
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144145929"
     variation       1818
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151022836"
     variation       1822
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140817788"
     variation       1823
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201495849"
     variation       1840
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201774749"
     variation       1847
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:34864600"
     variation       1881
                     /gene="DOCK2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:111348804"
     exon            1924..2021
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       1953
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149106608"
     variation       2004
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184460829"
     exon            2022..2111
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2063
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371790704"
     variation       2066
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368933125"
     exon            2112..2212
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2130
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35832136"
     variation       2162
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145746510"
     variation       2186
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75416239"
     exon            2213..2347
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2215
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368031697"
     variation       2279
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35530753"
     variation       2321
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35887608"
     variation       2322
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199603412"
     variation       2329
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373947127"
     variation       2330
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200305228"
     variation       2334
                     /gene="DOCK2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:371936048"
     exon            2348..2456
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2354
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138285820"
     variation       2358
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371785252"
     variation       2378
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372634514"
     variation       2432
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:13155521"
     variation       2433
                     /gene="DOCK2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:376374557"
     exon            2457..2527
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2472
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373025633"
     exon            2528..2634
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2539
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370192291"
     variation       2540
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146897720"
     variation       2600
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374883782"
     variation       2604
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372598080"
     variation       2605
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148384873"
     exon            2635..2783
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2658
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201511979"
     variation       2661
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369306554"
     variation       2667
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141501849"
     variation       2715
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150884555"
     variation       2718
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:112062072"
     variation       2735
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141649591"
     variation       2736
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199862297"
     exon            2784..2879
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2807
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:261623"
     variation       2837
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376912207"
     variation       2842
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370529585"
     variation       2862
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200070944"
     exon            2880..2978
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       2937
                     /gene="DOCK2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:144126398"
     variation       2938
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35395501"
     variation       2947
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188136128"
     exon            2979..3073
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3019
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148694888"
     variation       3026
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:36028557"
     exon            3074..3152
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3080
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151197976"
     variation       3098
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374774675"
     variation       3133
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201825096"
     variation       3136
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368028175"
     variation       3137
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:150071550"
     exon            3153..3253
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3220
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:145444170"
     variation       3227
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199995403"
     exon            3254..3312
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3271
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185160653"
     variation       3272
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:58980222"
     variation       3273
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368843643"
     variation       3275
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2287727"
     exon            3313..3461
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3339
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:187197739"
     variation       3351
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150196463"
     variation       3365
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138927937"
     variation       3391
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149008494"
     variation       3446
                     /gene="DOCK2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:200973349"
     exon            3462..3547
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3482
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143743514"
     variation       3494
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148138145"
     variation       3497
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149853735"
     variation       3515
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370111673"
     variation       3518
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181479183"
     variation       3536
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:9791113"
     exon            3548..3704
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3584
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:200201722"
     variation       3589
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:137955744"
     variation       3617..3618
                     /gene="DOCK2"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:34576936"
     variation       3679
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373428643"
     variation       3692
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3763048"
     exon            3705..3745
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     exon            3746..3836
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3763
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139600790"
     variation       3764
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149321142"
     variation       3777
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:193074993"
     variation       3821
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144649763"
     variation       3825
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139639543"
     variation       3828
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184632847"
     exon            3837..3956
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3891
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200108047"
     variation       3900
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377233075"
     variation       3901
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145262338"
     variation       3908
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:6555882"
     variation       3916
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145873210"
     variation       3917
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142249400"
     variation       3923
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:151251345"
     variation       3934
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369071999"
     exon            3957..4046
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       3968
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140468355"
     variation       3994
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370316549"
     variation       3995
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150482679"
     variation       4005
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146643993"
     variation       4025
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:34133853"
     variation       4031
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:145117786"
     exon            4047..4151
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4084
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:60146068"
     variation       4124
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199913251"
     exon            4152..4293
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4158
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:137922056"
     variation       4172
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142465529"
     variation       4231
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375716929"
     variation       4263
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201799740"
     variation       4281
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:143100569"
     exon            4294..4375
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4364
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76688275"
     exon            4376..4460
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4388
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141164963"
     variation       4394
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:17647491"
     variation       4421
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181184602"
     variation       4422
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200408270"
     variation       4432
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199755413"
     variation       4436
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139781718"
     exon            4461..4547
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4488
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143595882"
     variation       4508
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147192858"
     variation       4518
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374174531"
     variation       4535
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140777013"
     variation       4543
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149796867"
     exon            4548..4724
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4554
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371649588"
     variation       4591
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201320169"
     variation       4592
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376411478"
     variation       4603
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145786592"
     variation       4613
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:148502872"
     variation       4676
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372927020"
     variation       4715
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377205336"
     exon            4725..4808
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4753
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:13179480"
     variation       4755
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199737175"
     variation       4770
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199902117"
     variation       4781
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376091703"
     variation       4783
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:13179490"
     exon            4809..4946
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4874
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369880478"
     variation       4901
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377080151"
     variation       4904
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375128647"
     variation       4931
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375712443"
     variation       4934
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2270900"
     variation       4938
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142830212"
     exon            4947..5074
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       4958
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201318538"
     variation       4959
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368481515"
     variation       4976
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1045168"
     variation       5035
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113216049"
     variation       5039
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:145086586"
     variation       5056
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:139644615"
     exon            5075..5246
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       5082
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377100198"
     variation       5104
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201322810"
     variation       5107
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:150108225"
     variation       5119
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373168304"
     variation       5128
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184196863"
     variation       5129
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201405765"
     variation       5137
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377714619"
     variation       5138
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138544957"
     variation       5150
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:149235480"
     variation       5154
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373978300"
     variation       5159
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:146935890"
     variation       5167
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371229305"
     variation       5169
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201624889"
     variation       5171
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:138159817"
     variation       5209
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200684209"
     variation       5210
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143741887"
     variation       5234
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:147230385"
     variation       5245
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199698060"
     exon            5247..5367
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       5267
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147774003"
     variation       5297
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:148811648"
     variation       5306
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202096890"
     variation       5315
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201601393"
     variation       5318
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113012149"
     variation       5339
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138826774"
     variation       5348
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370450130"
     exon            5368..5510
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       5374
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141274816"
     variation       5375
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370911923"
     variation       5404
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:58570833"
     variation       5415
                     /gene="DOCK2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:2270898"
     variation       5424
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149343589"
     variation       5425
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376280359"
     variation       5441
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149976182"
     variation       5457
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146061014"
     variation       5470
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140044343"
     variation       5478
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368448938"
     variation       5482
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143896166"
     variation       5505
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146886839"
     exon            5511..6097
                     /gene="DOCK2"
                     /inference="alignment:Splign:1.39.8"
     variation       5519
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371835495"
     STS             5521..5709
                     /gene="DOCK2"
                     /standard_name="RH25421"
                     /db_xref="UniSTS:5858"
     variation       5525
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200128185"
     variation       5526
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144315682"
     variation       5555
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114098294"
     variation       5558
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:151161252"
     variation       5563
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202005409"
     variation       5564
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140198889"
     variation       5597
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369628471"
     variation       5640
                     /gene="DOCK2"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:55803405"
     variation       5665
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:183929574"
     variation       5672
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:187711257"
     variation       5731
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1045176"
     variation       5734
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:9307"
     variation       5761
                     /gene="DOCK2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:147788572"
     variation       5792
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:192346052"
     variation       5892
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:114945769"
     variation       5901
                     /gene="DOCK2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1045192"
     STS             5997..6096
                     /gene="DOCK2"
                     /standard_name="SGC32167"
                     /db_xref="UniSTS:82994"
     variation       6009
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376770574"
     variation       6017
                     /gene="DOCK2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:57495438"
     variation       6047
                     /gene="DOCK2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:184485182"
ORIGIN      
aggaaggaagtggggccctgcggcgcccagccaccccctgacggcttccccacgggaggacgcgaggccccggcccagccatggccccctggcgcaaagctgacaaggagcggcacggcgtggccatatacaacttccaaggcagcggagccccccagctctccctgcagatcggcgatgtggtgcgaatacaggagacgtgtggagactggtataggggatacctcataaagcacaaaatgttacagggcatttttcctaagtcatttatccacatcaaggaagtgacagttgagaaaagaagaaatactgagaacatcattcctgcagaaattcctctggcacaagaagtgacaacgacactttgggaatggggaagcatctggaaacaactctatgtggccagcaaaaaggagcgttttctccaggtgcagtccatgatgtacgatctgatggagtggaggtcccagcttctctcaggaaccttacccaaggatgagctgaaggaactgaagcagaaagtcacgtccaaaattgactatggcaacaaaatccttgagcttgatttgattgtcagagatgaagacggaaatatcttggaccctgataataccagtgtcatcagcttgttccatgcacatgaggaagcaactgataaaatcacagagcgtatcaaagaagaaatgtcaaaagaccagccagattatgcaatgtattcccggatctcctcatcccccacccatagcctctatgtgtttgtgagaaactttgtgtgcagaattggggaagatgctgagctcttcatgtctctctacgaccccaacaagcaaacggtcataagtgagaactacctagtgcgatggggcagccggggcttccctaaggagattgagatgctcaacaatctgaaggtggtcttcacggatcttggaaacaaagacctcaacagggataaaatttacttgatttgtcaaatagtccgggtcggcaagatggatcttaaggatactggtgcaaagaagtgcacgcagggactgaggaggccctttggggtggcagttatggatataacagacatcatcaaggggaaagcagagagtgatgaagaaaagcagcacttcattccttttcacccggttacagctgagaatgacttcctacacagcctgctgggcaaagtcatagcctccaagggggacagtggagggcaaggcctctgggtgaccatgaagatgctggtgggtgacatcattcagattcgcaaggactatccacacctggtggacaggaccaccgtggtggccaggaagctgggattcccagagatcatcatgccaggggatgtcaggaacgacatctacattactctcttacaaggtgactttgacaagtacaacaagaccacacagaggaatgtggaagtcatcatgtgtgtgtgcgcggaggatggcaaaacgctgcctaatgcaatttgcgtgggagcaggggacaagcccatgaatgagtatcgctccgttgtgtactatcaagtcaaacagccacgctggatggaaacagtcaaggtggctgtccctattgaagacatgcagaggatccatctgcgattcatgtttcgacatcggtcatctctggaatctaaagataaaggagaaaagaactttgccatgtcctatgtgaagctgatgaaagaagatgggactactctacacgatggattccatgacttagttgtcctcaagggggacagcaagaagatggaggatgccagcgcatacctgacccttccttcttatcgacaccatgtggaaaacaagggggccacgctgagcaggagctccagcagtgttggggggctttctgtcagctcccgggatgtgttctccatttccaccctggtgtgctccacaaagctcactcagaatgtgggcttgctgggtttgctgaagtggcgtatgaagcctcaactgctacaggagaatttagaaaagttgaagattgtggatggagaggaagtggtgaagtttctccaggatactctggatgccctcttcaacatcatgatggagcattctcaaagtgatgaatatgacatcctcgtctttgatgccttgatttacataataggactcattgcagaccggaaatttcagcatttcaacaccgttctggaggcttacatccaacagcatttcagtgcgaccttggcttacaagaaattgatgacagtgctgaagacttacttggatacctccagcagaggggagcaatgtgagccaatcctaagaacgctgaaggctttggaatatgtgttcaagttcattgttcggtcgaggacattattttcacagctttatgaaggcaaagaacagatggagtttgaagaatccatgagacggctctttgaatccatcaacaatctgatgaaaagtcaatacaaaactaccatccttttgcaggtggcggctttgaaatacatcccatctgtcctgcatgatgtagaaatggtctttgatgcgaagttactcagccaactcctgtatgagttctacacctgcatccctcctgtgaaactccagaagcagaaagtacagtctatgaatgagatagtccagagcaacctctttaaaaagcaagaatgccgggacattctgcttcctgtcatcaccaaagagctgaaggagctgctggagcagaaggatgacatgcaacaccaggtcctggagaggaagtactgcgttgaattgctcaacagcatcttggaagtccttagctaccaggatgcggccttcacctaccaccatatccaggagatcatggtccagctgctgcggacagtgaaccggacagtcatcaccatgggccgggatcacattctgattagtcactttgtggcatgtatgacagccatcttaaaccagatgggtgaccagcactactccttctacattgagaccttccagaccagctctgaacttgtggacttcttgatggagaccttcatcatgttcaaggacctcattggaaagaacgtgtaccctggagactggatggccatgagcatggttcaaaacagggtcttcctgagagctatcaacaagtttgcagaaaccatgaaccagaagttcctagaacacacgaactttgagttccagctgtggaacaactattttcatctggcagtggcttttatcacccaggattctctgcagctggagcagttctcacacgccaaatacaacaaaatcctgaataagtatggggacatgagacggctaattggcttctccatccgtgatatgtggtacaagcttggtcagaacaaaatctgcttcatcccaggcatggtaggacctatattagagatgacacttatccctgaggctgagctccggaaagccaccataccaatcttcttcgacatgatgctgtgtgaatatcaaagaagtggggatttcaaaaagtttgaaaacgaaatcatcctgaagctggaccacgaggtagaagggggccgaggcgacgagcagtacatgcagctcctggagtcaatcctgatggaatgtgctgcagagcacccaaccattgccaagtcggtggagaacttcgtgaacctggtcaaaggcctcctggagaagctgctggattaccggggtgtgatgacagatgagagcaaagacaaccgcatgagctgcaccgtgaacctgctgaatttctacaaagataacaacagggaggagatgtacataaggtacctgtacaaactccgcgatcttcacctggactgtgacaattacacagaggctgcctacacgctccttctccacacctggcttctcaagtggtcggatgagcagtgtgcatcacaggtcatgcagacaggccagcagcacccccagacacaccggcagctgaaggagacgctctacgagaccatcataggctactttgacaaaggaaagatgtgggaagaggccataagtctgtgcaaggagctggcggaacagtacgagatggagatctttgactatgagctgctcagccagaacctgatccagcaggcaaaattctatgaaagcatcatgaaaatcctcaggcccaaaccagactactttgctgttggatactacggccagggattcccctccttcctgcggaacaaagtgttcatctaccgcgggaaggaatatgagcgaagagaagatttccagatgcagctgatgacccagttccccaatgcagagaagatgaacaccacctctgccccgggagatgatgtgaagaatgccccaggccagtatatccagtgcttcactgtccagcctgtcttggatgaacatcccaggttcaagaataagccagtgcctgaccagattataaacttctacaaatccaactacgtgcaaaggttccactactcccggcccgtgcgcagggggaccgtagacccagagaatgagtttgcttccatgtggattgagagaacctccttcgtgactgcatacaagctgccggggatcctgcgctggtttgaggtggtgcacatgtcgcagaccacaattagtcctctggagaatgccatagaaaccatgtccacggccaatgagaagatcctgatgatgataaaccagtaccagagtgatgagaccctccccatcaacccactctccatgctcctgaacgggattgtggaccctgctgtcatgggaggcttcgccaagtatgagaaggccttcttcactgaagagtatgtcagggaccaccctgaggaccaggacaagctgacccacctcaaggacctgattgcatggcagatccccttcttgggagctgggattaagatccatgagaaaagggtgtcagataacttgcgacccttccatgaccggatggaggaatgtttcaagaacctgaaaatgaaggtggagaaggagtacggtgtccgagagatgcctgactttgacgacaggagagtgggccgtcccaggtctatgctgcgctcatacagacagatgtccatcatctctctggcttccatgaattctgactgcagcacccccagcaagcctacctcagagagctttgacctggaattagcatcacccaagacgccgagagtggagcaggaggaaccgatctccccggggagcaccctgcctgaggtcaagctgcggaggtccaagaagaggacaaagagaagcagcgtagtttttgcggatgagaaagcagctgcagagtcggacctgaagcggctttccaggaagcatgagttcatgagtgacaccaacctctcggagcatgcggccatccccctcaaggcgtctgtcctctctcaaatgagctttgccagccagtccatgcctaccatcccagccctggcgctctcagtggcaggcatccctgggttggatgaggccaacacatctccccgcctcagccagaccttcctccaactctcagatggtgacaagaagacactcacacggaagaaggtcaatcagttcttcaagacaatgctggccagcaaatcggctgaagaaggcaaacagatcccagactcgctgtccacggacctgtgagctgctgctgactagggctgcatgggagagccagggaggggagtttctggaagaggaaagccatgcgtggaacatcgaagcctcagagagtgggagactgtccccatcagttgtccttacttagaggagacagagaggccaatcaggtcccagagcttgaatgctaacaagcccagcatcccctggggctgtgatcatggtggatgaggaagcctcaacgtagattcctgaactcaaggtaccagcaagaatgccttctcccagtgtgctctccccaacatcctaggcacagctttcataacccagtttcttaggtgtaagaaactgtttttatctcatttattaagtctcagaacttaacagaaaaggaagccttttaaatattctttttaattttattttagattaacagttttgtactttacatttttttatacaaccaaccagtttcttttctagccaatcatctctgaagagttgctgtttcttactgacaataaaaaatgttctcttggttcgaataaaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:1794 -> Molecular function: GO:0009055 [electron carrier activity] evidence: IEA
            GeneID:1794 -> Molecular function: GO:0020037 [heme binding] evidence: IEA
            GeneID:1794 -> Molecular function: GO:0030675 [Rac GTPase activator activity] evidence: IEA
            GeneID:1794 -> Molecular function: GO:0030676 [Rac guanyl-nucleotide exchange factor activity] evidence: IDA
            GeneID:1794 -> Molecular function: GO:0042608 [T cell receptor binding] evidence: IDA
            GeneID:1794 -> Biological process: GO:0001766 [membrane raft polarization] evidence: IEA
            GeneID:1794 -> Biological process: GO:0001768 [establishment of T cell polarity] evidence: IEA
            GeneID:1794 -> Biological process: GO:0001771 [immunological synapse formation] evidence: IEA
            GeneID:1794 -> Biological process: GO:0002277 [myeloid dendritic cell activation involved in immune response] evidence: ISS
            GeneID:1794 -> Biological process: GO:0006935 [chemotaxis] evidence: IEA
            GeneID:1794 -> Biological process: GO:0007264 [small GTPase mediated signal transduction] evidence: IEA
            GeneID:1794 -> Biological process: GO:0016032 [viral process] evidence: TAS
            GeneID:1794 -> Biological process: GO:0030036 [actin cytoskeleton organization] evidence: TAS
            GeneID:1794 -> Biological process: GO:0044351 [macropinocytosis] evidence: ISS
            GeneID:1794 -> Biological process: GO:0045059 [positive thymic T cell selection] evidence: IEA
            GeneID:1794 -> Biological process: GO:0045060 [negative thymic T cell selection] evidence: IEA
            GeneID:1794 -> Biological process: GO:0046633 [alpha-beta T cell proliferation] evidence: IEA
            GeneID:1794 -> Biological process: GO:0050690 [regulation of defense response to virus by virus] evidence: TAS
            GeneID:1794 -> Biological process: GO:0050766 [positive regulation of phagocytosis] evidence: ISS
            GeneID:1794 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:1794 -> Cellular component: GO:0005856 [cytoskeleton] evidence: IEA
            GeneID:1794 -> Cellular component: GO:0012505 [endomembrane system] evidence: IEA
            GeneID:1794 -> Cellular component: GO:0016020 [membrane] evidence: IEA

by @meso_cacase at DBCLS
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