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2024-04-26 08:27:45, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001242644            3740 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens RAB2A, member RAS oncogene family (RAB2A), transcript
            variant 2, mRNA.
ACCESSION   NM_001242644 XR_108913
VERSION     NM_001242644.1  GI:336391092
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 3740)
  AUTHORS   de Barsy,M., Jamet,A., Filopon,D., Nicolas,C., Laloux,G.,
            Rual,J.F., Muller,A., Twizere,J.C., Nkengfac,B., Vandenhaute,J.,
            Hill,D.E., Salcedo,S.P., Gorvel,J.P., Letesson,J.J. and De Bolle,X.
  TITLE     Identification of a Brucella spp. secreted effector specifically
            interacting with human small GTPase Rab2
  JOURNAL   Cell. Microbiol. 13 (7), 1044-1058 (2011)
   PUBMED   21501366
  REMARK    GeneRIF: The authors identified a specific interaction between the
            human small GTPase Rab2 and a Brucella spp. protein named RicA.
REFERENCE   2  (bases 1 to 3740)
  AUTHORS   Buffa,L., Fuchs,E., Pietropaolo,M., Barr,F. and Solimena,M.
  TITLE     ICA69 is a novel Rab2 effector regulating ER-Golgi trafficking in
            insulinoma cells
  JOURNAL   Eur. J. Cell Biol. 87 (4), 197-209 (2008)
   PUBMED   18187231
  REMARK    GeneRIF: ICA69 as a novel Rab2 effector and its role in regulating
            the early transport of insulin secretory granule proteins
REFERENCE   3  (bases 1 to 3740)
  AUTHORS   Dong,C. and Wu,G.
  TITLE     Regulation of anterograde transport of adrenergic and angiotensin
            II receptors by Rab2 and Rab6 GTPases
  JOURNAL   Cell. Signal. 19 (11), 2388-2399 (2007)
   PUBMED   17716866
  REMARK    GeneRIF: These data demonstrate that Rab2 and Rab6 differentially
            influence anterograde transport and signaling of GPCRs.
REFERENCE   4  (bases 1 to 3740)
  AUTHORS   Chi,A., Valencia,J.C., Hu,Z.Z., Watabe,H., Yamaguchi,H.,
            Mangini,N.J., Huang,H., Canfield,V.A., Cheng,K.C., Yang,F., Abe,R.,
            Yamagishi,S., Shabanowitz,J., Hearing,V.J., Wu,C., Appella,E. and
            Hunt,D.F.
  TITLE     Proteomic and bioinformatic characterization of the biogenesis and
            function of melanosomes
  JOURNAL   J. Proteome Res. 5 (11), 3135-3144 (2006)
   PUBMED   17081065
REFERENCE   5  (bases 1 to 3740)
  AUTHORS   Eathiraj,S., Pan,X., Ritacco,C. and Lambright,D.G.
  TITLE     Structural basis of family-wide Rab GTPase recognition by
            rabenosyn-5
  JOURNAL   Nature 436 (7049), 415-419 (2005)
   PUBMED   16034420
REFERENCE   6  (bases 1 to 3740)
  AUTHORS   de Leeuw,H.P., Koster,P.M., Calafat,J., Janssen,H., van
            Zonneveld,A.J., van Mourik,J.A. and Voorberg,J.
  TITLE     Small GTP-binding proteins in human endothelial cells
  JOURNAL   Br. J. Haematol. 103 (1), 15-19 (1998)
   PUBMED   9792283
REFERENCE   7  (bases 1 to 3740)
  AUTHORS   Tisdale,E.J. and Balch,W.E.
  TITLE     Rab2 is essential for the maturation of pre-Golgi intermediates
  JOURNAL   J. Biol. Chem. 271 (46), 29372-29379 (1996)
   PUBMED   8910601
REFERENCE   8  (bases 1 to 3740)
  AUTHORS   Khosravi-Far,R., Lutz,R.J., Cox,A.D., Conroy,L., Bourne,J.R.,
            Sinensky,M., Balch,W.E., Buss,J.E. and Der,C.J.
  TITLE     Isoprenoid modification of rab proteins terminating in CC or CXC
            motifs
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 88 (14), 6264-6268 (1991)
   PUBMED   1648736
REFERENCE   9  (bases 1 to 3740)
  AUTHORS   Zahraoui,A., Touchot,N., Chardin,P. and Tavitian,A.
  TITLE     The human Rab genes encode a family of GTP-binding proteins related
            to yeast YPT1 and SEC4 products involved in secretion
  JOURNAL   J. Biol. Chem. 264 (21), 12394-12401 (1989)
   PUBMED   2501306
REFERENCE   10 (bases 1 to 3740)
  AUTHORS   Tachibana,K., Umezawa,A., Kato,S. and Takano,T.
  TITLE     Nucleotide sequence of a new YPT1-related human cDNA which belongs
            to the ras gene superfamily
  JOURNAL   Nucleic Acids Res. 16 (21), 10368 (1988)
   PUBMED   3057444
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DA648682.1, AK297576.1,
            AC068389.10 and AW301641.1.
            On Jun 19, 2011 this sequence version replaced gi:310120219.
            
            Summary: The protein encoded by this gene belongs to the Rab
            family, members of which are small molecular weight guanosine
            triphosphatases (GTPases) that contain highly conserved domains
            involved in GTP binding and hydrolysis. The Rabs are membrane-bound
            proteins, involved in vesicular fusion and trafficking. This
            protein is a resident of pre-Golgi intermediates, and is required
            for protein transport from the endoplasmic reticulum (ER) to the
            Golgi complex. Alternatively spliced transcript variants encoding
            different isoforms have been found for this gene. [provided by
            RefSeq, Oct 2011].
            
            Transcript Variant: This variant (2) lacks an in-frame exon in the
            5' coding region compared to variant 1. This results in a shorter
            isoform (b) missing an internal protein segment compared to isoform
            a.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            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 :: AK297576.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025098 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-322               DA648682.1         3-324
            323-1084            AK297576.1         297-1058
            1085-2055           AC068389.10        53096-54066         c
            2056-3281           AC068389.10        51870-53095         c
            3282-3740           AW301641.1         1-459               c
FEATURES             Location/Qualifiers
     source          1..3740
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="8"
                     /map="8q12.1"
     gene            1..3740
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="RAB2A, member RAS oncogene family"
                     /db_xref="GeneID:5862"
                     /db_xref="HGNC:9763"
                     /db_xref="MIM:179509"
     exon            1..344
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /inference="alignment:Splign:1.39.8"
     variation       8
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:13248794"
     variation       35
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188897877"
     variation       71
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377019145"
     variation       180
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11544472"
     variation       238
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79202491"
     variation       269
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370633697"
     misc_feature    284..286
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="upstream in-frame stop codon"
     CDS             299..865
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="isoform b is encoded by transcript variant 2; RAB2,
                     member RAS oncogene family; ras-related protein Rab-2A;
                     small GTP binding protein RAB2A"
                     /codon_start=1
                     /product="ras-related protein Rab-2A isoform b"
                     /protein_id="NP_001229573.1"
                     /db_xref="GI:336391093"
                     /db_xref="CCDS:CCDS56537.1"
                     /db_xref="GeneID:5862"
                     /db_xref="HGNC:9763"
                     /db_xref="MIM:179509"
                     /translation="
MAYAYLFKYIIIGDTGVEFGARMITIDGKQIKLQIWDTAGQESFRSITRSYYRGAAGALLVYDITRRDTFNHLTTWLEDARQHSNSNMVIMLIGNKSDLESRREVKKEEGEAFAREHGLIFMETSAKTASNVEEAFINTAKEIYEKIQEGVFDINNEANGIKIGPQHAATNATHAGNQGGQQAGGGCC
"
     misc_feature    305..736
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="Rat sarcoma (Ras)-like superfamily of small
                     guanosine triphosphatases (GTPases); Region:
                     Ras_like_GTPase; cl17170"
                     /db_xref="CDD:247724"
     misc_feature    order(341..343,416..418,581..586,590..592,671..679)
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="GTP/Mg2+ binding site [chemical binding]; other
                     site"
                     /db_xref="CDD:206648"
     misc_feature    350..358
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="Switch I region; other site"
                     /db_xref="CDD:206648"
     misc_feature    407..418
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="G3 box; other site"
                     /db_xref="CDD:206648"
     misc_feature    order(413..418,464..469)
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="Switch II region; other site"
                     /db_xref="CDD:206648"
     misc_feature    581..592
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="G4 box; other site"
                     /db_xref="CDD:206648"
     misc_feature    671..679
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /note="G5 box; other site"
                     /db_xref="CDD:206648"
     variation       307
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373226742"
     exon            345..412
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /inference="alignment:Splign:1.39.8"
     variation       355
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368402545"
     exon            413..495
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /inference="alignment:Splign:1.39.8"
     variation       450
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11544470"
     exon            496..588
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /inference="alignment:Splign:1.39.8"
     variation       502
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375530419"
     exon            589..700
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /inference="alignment:Splign:1.39.8"
     variation       613
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:141013917"
     variation       655
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370866047"
     variation       656
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199581780"
     exon            701..769
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /inference="alignment:Splign:1.39.8"
     exon            770..3740
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /inference="alignment:Splign:1.39.8"
     STS             773..907
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="STS-R00195"
                     /db_xref="UniSTS:16383"
     STS             778..908
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="RH70011"
                     /db_xref="UniSTS:5095"
     variation       853
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370628676"
     variation       854
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374486741"
     STS             856..1353
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="RAB2_2543"
                     /db_xref="UniSTS:280950"
     STS             874..1149
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="D8S1929"
                     /db_xref="UniSTS:76818"
     variation       892
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367660654"
     variation       893
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201836844"
     variation       910
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368529941"
     polyA_signal    1012..1017
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     polyA_site      1037
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     variation       1128
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:183524386"
     variation       1209
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:187759374"
     variation       1231
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:76823768"
     variation       1258..1259
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace=""
                     /replace="tt"
                     /db_xref="dbSNP:200305948"
     variation       1293
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:41272433"
     variation       1396
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370058692"
     variation       1497
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:113877343"
     variation       1534
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374973250"
     variation       1636
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79502934"
     variation       1759
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:77133934"
     STS             1825..1976
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="D8S1899"
                     /db_xref="UniSTS:22645"
     STS             1825..1948
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="RH92689"
                     /db_xref="UniSTS:92717"
     variation       1904..1905
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:35329667"
     STS             1918..2023
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="D8S1405E"
                     /db_xref="UniSTS:151199"
     variation       1938
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140580809"
     polyA_signal    1947..1952
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     variation       1965
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7413"
     polyA_site      1976
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     polyA_signal    2075..2080
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     polyA_site      2095
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     variation       2204
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369628178"
     variation       2246
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373337569"
     variation       2339
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12544487"
     variation       2381
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78628010"
     variation       2432
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:629268"
     variation       2508
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:150407587"
     variation       2541
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:79970848"
     variation       2662
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:649634"
     variation       2731
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138129268"
     variation       2758
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:192628540"
     variation       2816
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:75837686"
     variation       2904
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2930041"
     STS             2930..3180
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="D8S1613"
                     /db_xref="UniSTS:79309"
     variation       2950
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:149557425"
     variation       2954
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:9437"
     variation       2998
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:118165570"
     variation       3002
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75974140"
     STS             3006..3190
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /standard_name="D8S1394E"
                     /db_xref="UniSTS:45049"
     variation       3118
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186973869"
     polyA_signal    3163..3168
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     variation       3182
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:145073984"
     polyA_site      3192
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     variation       3240
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76705987"
     variation       3246
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:652422"
     variation       3260
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:138862634"
     variation       3284
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374444619"
     variation       3331
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142611281"
     variation       3338
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:113076295"
     variation       3344
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:191757602"
     variation       3358
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113490250"
     variation       3427
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:184729393"
     variation       3601
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116372466"
     variation       3635
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189591638"
     variation       3644
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181704218"
     polyA_signal    3702..3707
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     variation       3715
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185297839"
     polyA_site      3733
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
     variation       3740
                     /gene="RAB2A"
                     /gene_synonym="LHX; RAB2"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:664796"
ORIGIN      
tttcctccggcggcgccggcggccgcagaacttccgggtcggcgcggaggcggggcggaggcgccgcggcggctgttattgttcggctgggctcggtcgggcgctgtctccctcggctctgcgggtgtcagttcgtccggcttcctcacagcccctcactcccggcggctgacagcagcagcggcggcggcgggcggcgcctggcgtttcgaggctgagcggcaccggggttggggcgcggaggaggagcagcagcgggaggaggagccgtgtgccctggcactgagcggccgcggccatggcgtacgcctatctcttcaagtacatcataatcggcgacacaggtgtagagttcggtgctcgaatgataactattgatgggaaacagataaaacttcagatatgggatacggcagggcaagaatcctttcgttccatcacaaggtcgtattacagaggtgcagcaggagctttactagtttacgatattacacggagagatacattcaaccacttgacaacctggttagaagatgcccgccagcattccaattccaacatggtcattatgcttattggaaataaaagtgatttagaatctagaagagaagtaaaaaaagaagaaggtgaagcttttgcacgagaacatggactcatcttcatggaaacgtctgctaagactgcttccaatgtagaagaggcatttattaatacagcaaaagaaatttatgaaaaaattcaagaaggagtctttgacattaataatgaggcaaatggcattaaaattggccctcagcatgctgctaccaatgcaacacatgcaggcaatcagggaggacagcaggctgggggcggctgctgttgagtctgtttttactgtctagctgcccaacggggcctactcacttattctttcaccccctctcctcctgctcagctgagacatgaaactatttgaaatggctttatgtcacagaagactttaatccgtcaaattcttgtataactttgaataaatggttaatgttcacttaaaagacagattttggagattgtattcatatctatttgcatttgatttctaggtcaattgatgtgattatttttgttaaatgttgtcttgtgcccttaactacgaactgaattgtattaaacactacaaagtcatcttgagtattttaaatcggtttgtgtagttaggtttcccaacatctgtggttacctaatgtttaatattatagaactgtcctcagaaactttgtcaattttcacggctataaggaaacagaaggactcttttaattctgtatttatcatttactttctgtatatatagtttaataacctgcttgggtgtaatttgccaagcttgaattctttaatgcatttgcataaattctatactgtttagagcttaaagctacagaagcattgttaggaattgcttggacactgaattttaaactttttgacattgttaacaagcatgttcatcttttcttgtcactagtccaagaaaaatatgcttaatgtatattacaaaggctttgtatatgttaacctgttttaatgccaaaagtttgctttgtccacaatttccttaagacctcttcagaaagggatttgtttgccttaatgaatactgttgggaaaaaacacagtataatgagtgaaaagggcagaagcaagaaatttctacatcttagcgactccaagaagaatgagtatccacatttagatggcacattatgaggactttaatctttccttaaacacaataatgttttcttttttcttttattcacatgatttctaagtatatttttcatgcaggacagtttttcaaccttgatgtacagtgactgtgtaaaatttttctttcagtggcaacctctataatctttaaaatatggtgagcatcttgtctgttttgaaggggatatgacaataaatctatcagatggaaaatcctgttacaaagtagaaaagctttagtaatttactcagtgtggtggttttatcctttttttctttttctcccttggtctataatgaaattgttacagcagtgcaaaataaaatcctatgtataaaagtgttctttttttttattatgaccacctcttttttaatgtatttttagtccacttacagcttttacatgggtttaagcatgttttttaaaagggtcagaatggttaacactcaaccctttttaaaaattttgctaaaatgcgacaaatctcaccatactgaaattatttttgttgatggtgtaagcagtgtaagcaagtgttttctcctgaactagcacaaaagcacttatgcctgaaagaaagcataaagaagttctaactctgaaactaactactttcatttcgctcatggccttcaactttctacaggtcttccctgaagattcagcagtactctctcaaaggtttgacagtactcttgtgggaaatcaccaaatgctgtcatagttttgttttaactgtctccttgagggcagagggaagggtgagagaaaatctgttttcatgggtatttgtagtacagcctttttttctttcaagtggctgtatcaaattcactggtcttactaatcactgtctttaccagtgagtacaaaaagttaaggcaactaggacaggtactgctctataccaagaagagaatgattctttggaaattgttatttttaagcttctgttaatttttccagaagtttagtgcgtttcttttccatactttctcccctaattcttttatttgaagaagagaacttaatggcaaataaacaacaaaccaggacatgcattttaataccctaaggaaaaatggaaccctcaaatataactcctcccacaaccaccctaatgtgcctcagtctggggcagcaggtggacttctcaatagttcttttccacattctctacaaatcacatctaccgttaaggaatatgttatgaatcctttctgttaattgagaaagcaatgttattgtctgtgatttccagtctttgctcattttattatccctgtcaaataatgtaatattggtacctgcagttgaatttgtaatattgtaattgaatttttagttgatcttcgatcagtttttatagcatctatggacatagaaaatcagtcactgaaaaaaataaacacagctttcaatgtctcactcaacatgtaacattcaaaattgtgatcttcataaagacattgttaccattcgtcttgcaaatttaagacaactgaatgaaaagccaattttttgaaagaatgtggcatataattagatatacaactgaaacaggatatacaactgcatacaatttgtttttaatgatattttaaaatagcctgttagcaggaaaatagtccctatttatctgctaatggtcaaaaagagttaggatataaatcgtaccaaaatgtttccaatcactcagaaaaactgattcatgtctggctttgcaacaccttaaacatttattctgtcatagatagtaaagccccatctcagtttatttagtcctgaggttggcagcatggggtttgactatatgagctaaaagatacacaaagagataacgctgtttcataataaacaggaattgactatacaaataggtaaaccagcatatctacctgtatttctcagagtttagatgtgtgctttatgtttacattaaaataaagcctaacgccacagtagatcatctcatactgca
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:5862 -> Molecular function: GO:0003924 [GTPase activity] evidence: IDA
            GeneID:5862 -> Molecular function: GO:0005525 [GTP binding] evidence: IDA
            GeneID:5862 -> Molecular function: GO:0019003 [GDP binding] evidence: IDA
            GeneID:5862 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
            GeneID:5862 -> Biological process: GO:0006184 [GTP catabolic process] evidence: IDA
            GeneID:5862 -> Biological process: GO:0006184 [GTP catabolic process] evidence: TAS
            GeneID:5862 -> Biological process: GO:0006888 [ER to Golgi vesicle-mediated transport] evidence: TAS
            GeneID:5862 -> Biological process: GO:0007264 [small GTPase mediated signal transduction] evidence: IEA
            GeneID:5862 -> Biological process: GO:0015031 [protein transport] evidence: IEA
            GeneID:5862 -> Cellular component: GO:0000139 [Golgi membrane] evidence: TAS
            GeneID:5862 -> Cellular component: GO:0005789 [endoplasmic reticulum membrane] evidence: IEA
            GeneID:5862 -> Cellular component: GO:0033116 [endoplasmic reticulum-Golgi intermediate compartment membrane] evidence: IEA
            GeneID:5862 -> Cellular component: GO:0042470 [melanosome] evidence: IEA

by @meso_cacase at DBCLS
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