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2019-03-25 14:57:42, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_004389               4005 bp    mRNA    linear   PRI 07-JUL-2013
DEFINITION  Homo sapiens catenin (cadherin-associated protein), alpha 2
            (CTNNA2), transcript variant 1, mRNA.
ACCESSION   NM_004389
VERSION     NM_004389.3  GI:259013214
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 4005)
  AUTHORS   Sherva R, Tripodis Y, Bennett DA, Chibnik LB, Crane PK, de Jager
            PL, Farrer LA, Saykin AJ, Shulman JM and Green RC.
  CONSRTM   The GENAROADS Consortium, and The Alzheimer's Disease Neuroimaging
            Initiative
  TITLE     Genome-wide association study of the rate of cognitive decline in
            Alzheimer's disease
  JOURNAL   Alzheimers Dement (2013) In press
   PUBMED   23535033
  REMARK    Publication Status: Available-Online prior to print
REFERENCE   2  (bases 1 to 4005)
  AUTHORS   Kask,M., Pruunsild,P. and Timmusk,T.
  TITLE     Bidirectional transcription from human LRRTM2/CTNNA1 and
            LRRTM1/CTNNA2 gene loci leads to expression of N-terminally
            truncated CTNNA1 and CTNNA2 isoforms
  JOURNAL   Biochem. Biophys. Res. Commun. 411 (1), 56-61 (2011)
   PUBMED   21708131
REFERENCE   3  (bases 1 to 4005)
  AUTHORS   Terracciano,A., Esko,T., Sutin,A.R., de Moor,M.H., Meirelles,O.,
            Zhu,G., Tanaka,T., Giegling,I., Nutile,T., Realo,A., Allik,J.,
            Hansell,N.K., Wright,M.J., Montgomery,G.W., Willemsen,G.,
            Hottenga,J.J., Friedl,M., Ruggiero,D., Sorice,R., Sanna,S.,
            Cannas,A., Raikkonen,K., Widen,E., Palotie,A., Eriksson,J.G.,
            Cucca,F., Krueger,R.F., Lahti,J., Luciano,M., Smoller,J.W., van
            Duijn,C.M., Abecasis,G.R., Boomsma,D.I., Ciullo,M., Costa,P.T. Jr.,
            Ferrucci,L., Martin,N.G., Metspalu,A., Rujescu,D., Schlessinger,D.
            and Uda,M.
  TITLE     Meta-analysis of genome-wide association studies identifies common
            variants in CTNNA2 associated with excitement-seeking
  JOURNAL   Transl Psychiatry 1, E49 (2011)
   PUBMED   22833195
  REMARK    GeneRIF: Common variants in CTNNA2 are associated with
            excitement-seeking and risk-taking.
            Publication Status: Online-Only
REFERENCE   4  (bases 1 to 4005)
  AUTHORS   Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B,
            Yusuf S, Gerstein HC, Engert JC 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   5  (bases 1 to 4005)
  AUTHORS   Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt
            TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M,
            Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ,
            Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S,
            Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD,
            Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE
            and Hingorani AD.
  CONSRTM   ASCOT investigators; NORDIL investigators; BRIGHT Consortium
  TITLE     Gene-centric association signals for lipids and apolipoproteins
            identified via the HumanCVD BeadChip
  JOURNAL   Am. J. Hum. Genet. 85 (5), 628-642 (2009)
   PUBMED   19913121
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   6  (bases 1 to 4005)
  AUTHORS   Bogaerts,S., Vanlandschoot,A., van Hengel,J. and van Roy,F.
  TITLE     Nuclear translocation of alphaN-catenin by the novel zinc finger
            transcriptional repressor ZASC1
  JOURNAL   Exp. Cell Res. 311 (1), 1-13 (2005)
   PUBMED   16182284
REFERENCE   7  (bases 1 to 4005)
  AUTHORS   Krauss,R.S., Cole,F., Gaio,U., Takaesu,G., Zhang,W. and Kang,J.S.
  TITLE     Close encounters: regulation of vertebrate skeletal myogenesis by
            cell-cell contact
  JOURNAL   J. Cell. Sci. 118 (PT 11), 2355-2362 (2005)
   PUBMED   15923648
  REMARK    Review article
REFERENCE   8  (bases 1 to 4005)
  AUTHORS   Hillier,L.W., Graves,T.A., Fulton,R.S., Fulton,L.A., Pepin,K.H.,
            Minx,P., Wagner-McPherson,C., Layman,D., Wylie,K., Sekhon,M.,
            Becker,M.C., Fewell,G.A., Delehaunty,K.D., Miner,T.L., Nash,W.E.,
            Kremitzki,C., Oddy,L., Du,H., Sun,H., Bradshaw-Cordum,H., Ali,J.,
            Carter,J., Cordes,M., Harris,A., Isak,A., van Brunt,A., Nguyen,C.,
            Du,F., Courtney,L., Kalicki,J., Ozersky,P., Abbott,S.,
            Armstrong,J., Belter,E.A., Caruso,L., Cedroni,M., Cotton,M.,
            Davidson,T., Desai,A., Elliott,G., Erb,T., Fronick,C., Gaige,T.,
            Haakenson,W., Haglund,K., Holmes,A., Harkins,R., Kim,K.,
            Kruchowski,S.S., Strong,C.M., Grewal,N., Goyea,E., Hou,S., Levy,A.,
            Martinka,S., Mead,K., McLellan,M.D., Meyer,R., Randall-Maher,J.,
            Tomlinson,C., Dauphin-Kohlberg,S., Kozlowicz-Reilly,A., Shah,N.,
            Swearengen-Shahid,S., Snider,J., Strong,J.T., Thompson,J.,
            Yoakum,M., Leonard,S., Pearman,C., Trani,L., Radionenko,M.,
            Waligorski,J.E., Wang,C., Rock,S.M., Tin-Wollam,A.M., Maupin,R.,
            Latreille,P., Wendl,M.C., Yang,S.P., Pohl,C., Wallis,J.W.,
            Spieth,J., Bieri,T.A., Berkowicz,N., Nelson,J.O., Osborne,J.,
            Ding,L., Meyer,R., Sabo,A., Shotland,Y., Sinha,P., Wohldmann,P.E.,
            Cook,L.L., Hickenbotham,M.T., Eldred,J., Williams,D., Jones,T.A.,
            She,X., Ciccarelli,F.D., Izaurralde,E., Taylor,J., Schmutz,J.,
            Myers,R.M., Cox,D.R., Huang,X., McPherson,J.D., Mardis,E.R.,
            Clifton,S.W., Warren,W.C., Chinwalla,A.T., Eddy,S.R., Marra,M.A.,
            Ovcharenko,I., Furey,T.S., Miller,W., Eichler,E.E., Bork,P.,
            Suyama,M., Torrents,D., Waterston,R.H. and Wilson,R.K.
  TITLE     Generation and annotation of the DNA sequences of human chromosomes
            2 and 4
  JOURNAL   Nature 434 (7034), 724-731 (2005)
   PUBMED   15815621
REFERENCE   9  (bases 1 to 4005)
  AUTHORS   Claverie,J.M., Hardelin,J.P., Legouis,R., Levilliers,J.,
            Bougueleret,L., Mattei,M.G. and Petit,C.
  TITLE     Characterization and chromosomal assignment of a human cDNA
            encoding a protein related to the murine 102-kDa
            cadherin-associated protein (alpha-catenin)
  JOURNAL   Genomics 15 (1), 13-20 (1993)
   PUBMED   8432524
REFERENCE   10 (bases 1 to 4005)
  AUTHORS   Hirano,S., Kimoto,N., Shimoyama,Y., Hirohashi,S. and Takeichi,M.
  TITLE     Identification of a neural alpha-catenin as a key regulator of
            cadherin function and multicellular organization
  JOURNAL   Cell 70 (2), 293-301 (1992)
   PUBMED   1638632
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            DC341423.1, DA313393.1, BC052996.1, BC040458.1 and BX648368.1.
            On Sep 22, 2009 this sequence version replaced gi:55770845.
            
            Transcript Variant: This variant (1) represents the longer
            transcript and encodes the longer isoform (1).
            
            CCDS Note: The coding region has been updated to remove a 3-nt
            insert (encoding Ser-310) that was present in the NCBI Build 36
            reference genome assembly. This insert has been removed in the
            GRCh37 reference genome, and its absence is supported by transcript
            data.
            
            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 :: BC052996.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025082, ERS025084 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-62                DC341423.1         1-62
            63-141              DA313393.1         1-79
            142-2210            BC052996.1         76-2144
            2211-2211           BC040458.1         1883-1883
            2212-3905           BC052996.1         2146-3839
            3906-4005           BX648368.1         1720-1819
FEATURES             Location/Qualifiers
     source          1..4005
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="2"
                     /map="2p12-p11.1"
     gene            1..4005
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /note="catenin (cadherin-associated protein), alpha 2"
                     /db_xref="GeneID:1496"
                     /db_xref="HGNC:2510"
                     /db_xref="MIM:114025"
     exon            1..274
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       33
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371130830"
     variation       72
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:146828435"
     variation       136
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139347248"
     exon            275..381
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     CDS             280..2997
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /note="isoform 1 is encoded by transcript variant 1;
                     cancer/testis antigen 114; catenin alpha-2;
                     alpha-N-catenin; cadherin-associated protein, related;
                     alpha N-catenin; alpha-catenin-related protein"
                     /codon_start=1
                     /product="catenin alpha-2 isoform 1"
                     /protein_id="NP_004380.2"
                     /db_xref="GI:55770846"
                     /db_xref="CCDS:CCDS42703.2"
                     /db_xref="GeneID:1496"
                     /db_xref="HGNC:2510"
                     /db_xref="MIM:114025"
                     /translation="
MTSATSPIILKWDPKSLEIRTLTVERLLEPLVTQVTTLVNTSNKGPSGKKKGRSKKAHVLAASVEQATQNFLEKGEQIAKESQDLKEELVAAVEDVRKQGETMRIASSEFADDPCSSVKRGTMVRAARALLSAVTRLLILADMADVMRLLSHLKIVEEALEAVKNATNEQDLANRFKEFGKEMVKLNYVAARRQQELKDPHCRDEMAAARGALKKNATMLYTASQAFLRHPDVAATRANRDYVFKQVQEAIAGISNAAQATSPTDEAKGHTGIGELAAALNEFDNKIILDPMTFSEARFRPSLEERLESIISGAALMADSSCTRDDRRERIVAECNAVRQALQDLLSEYMNNTGRKEKGDPLNIAIDKMTKKTRDLRRQLRKAVMDHISDSFLETNVPLLVLIEAAKSGNEKEVKEYAQVFREHANKLVEVANLACSISNNEEGVKLVRMAATQIDSLCPQVINAALTLAARPQSKVAQDNMDVFKDQWEKQVRVLTEAVDDITSVDDFLSVSENHILEDVNKCVIALQEGDVDTLDRTAGAIRGRAARVIHIINAEMENYEAGVYTEKVLEATKLLSETVMPRFAEQVEVAIEALSANVPQPFEENEFIDASRLVYDGVRDIRKAVLMIRTPEELEDDSDFEQEDYDVRSRTSVQTEDDQLIAGQSARAIMAQLPQEEKAKIAEQVEIFHQEKSKLDAEVAKWDDSGNDIIVLAKQMCMIMMEMTDFTRGKGPLKNTSDVINAAKKIAEAGSRMDKLARAVADQCPDSACKQDLLAYLQRIALYCHQLNICSKVKAEVQNLGGELIVSGLDSATSLIQAAKNLMNAVVLTVKASYVASTKYQKVYGTAAVNSPVVSWKMKAPEKKPLVKREKPEEFQTRVRRGSQKKHISPVQALSEFKAMDSF
"
     misc_feature    331..2877
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /note="Vinculin family; Region: Vinculin; pfam01044"
                     /db_xref="CDD:216263"
     misc_feature    1063..1065
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    2197..2199
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    2236..2238
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    2239..2241
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    2836..2838
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     variation       288
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368717286"
     variation       292
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372730685"
     variation       299
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190886290"
     variation       328
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375583816"
     variation       341
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369692132"
     exon            382..577
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       513
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200093329"
     variation       514
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377364195"
     variation       529
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:370052135"
     variation       558
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200888828"
     variation       568
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373818447"
     variation       569
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376745664"
     exon            578..744
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       585
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373823087"
     variation       595
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200794947"
     variation       603
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367585575"
     variation       630
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201020471"
     variation       640
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372361564"
     variation       645
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375393951"
     variation       656
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368392741"
     variation       657
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372587283"
     variation       665
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:377081241"
     variation       677
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141412774"
     variation       678
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:61754544"
     exon            745..864
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       747
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369887746"
     variation       753
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:199898826"
     exon            865..1131
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       887
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372749015"
     variation       903
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375699264"
     variation       904
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:370270410"
     variation       945
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:202210209"
     variation       948
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189010355"
     variation       979
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371032975"
     variation       984
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:61291641"
     variation       1032
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368210973"
     variation       1035
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76801084"
     variation       1062
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376731072"
     variation       1074
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202127694"
     variation       1075
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139544972"
     variation       1091
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371923353"
     exon            1132..1335
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       1183
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377243520"
     variation       1203..1204
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="agc"
                     /db_xref="dbSNP:10578220"
     variation       1204..1206
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="agc"
                     /db_xref="dbSNP:141716387"
     variation       1205
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200453143"
     variation       1207..1208
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="gca"
                     /db_xref="dbSNP:35072200"
     variation       1207..1208
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:79358881"
     variation       1218
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370498426"
     variation       1241
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:13004023"
     variation       1242
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373147177"
     variation       1272
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112183183"
     variation       1317
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200844323"
     exon            1336..1416
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       1355
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:373365115"
     variation       1370
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61754542"
     variation       1373
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369970894"
     exon            1417..1569
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       1466
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:144724508"
     variation       1479
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35181295"
     variation       1496
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:376103479"
     variation       1503
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148134866"
     exon            1570..1662
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       1637
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372299559"
     exon            1663..1819
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       1670
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372130983"
     variation       1674
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199835264"
     variation       1677
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183388824"
     variation       1683
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368093118"
     variation       1745
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201409476"
     variation       1752
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:371922258"
     variation       1774
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376635234"
     variation       1776
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200693218"
     variation       1795
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368671776"
     variation       1809
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:35760472"
     exon            1820..2020
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       1825
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372762175"
     variation       1878
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:34741453"
     variation       1890
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2304338"
     variation       1892
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374311367"
     variation       1893
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:374667703"
     variation       1963
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199781520"
     exon            2021..2172
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       2029
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200341629"
     variation       2050
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376734623"
     variation       2059
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367957293"
     variation       2076
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371544995"
     variation       2079
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2228460"
     variation       2081
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150870808"
     variation       2083
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:199851508"
     variation       2088
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370004446"
     variation       2149
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373816978"
     variation       2155
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375218627"
     variation       2161
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369395759"
     exon            2173..2286
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       2193
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200688682"
     variation       2211
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:17854795"
     variation       2231
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:61743764"
     variation       2280
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368214934"
     exon            2287..2468
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       2307
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:199921745"
     variation       2380
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:41288785"
     variation       2457
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:140894812"
     exon            2469..2574
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       2475
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200977623"
     exon            2575..2709
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       2691
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:369818338"
     variation       2694
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372072591"
     exon            2710..3993
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /inference="alignment:Splign:1.39.8"
     variation       2724
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369006211"
     variation       2764
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201128941"
     variation       2767
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:139367648"
     variation       2772
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377763685"
     variation       2924
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:202053681"
     STS             2975..3217
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /standard_name="G10614"
                     /db_xref="UniSTS:63953"
     variation       3000
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:189634424"
     variation       3001
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375801955"
     variation       3013
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:377284441"
     variation       3027..3030
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="cttt"
                     /db_xref="dbSNP:375870913"
     variation       3051
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:78913430"
     variation       3115
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181635078"
     variation       3132
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:186768234"
     STS             3134..3831
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /standard_name="CTNNA2_567"
                     /db_xref="UniSTS:468364"
     variation       3146
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:146155710"
     variation       3169
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:377148303"
     variation       3259
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370523708"
     variation       3267
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373715823"
     STS             3286..3630
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /standard_name="WI-7682"
                     /db_xref="UniSTS:52048"
     variation       3291
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11555661"
     variation       3344
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:138787272"
     variation       3430
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201213456"
     STS             3453..3598
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /standard_name="RH66010"
                     /db_xref="UniSTS:89466"
     variation       3503
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141978801"
     variation       3505
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:60296403"
     variation       3611
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11445"
     variation       3697
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76851105"
     variation       3716..3717
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:200455804"
     variation       3717
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:372255835"
     variation       3726..3727
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:34088328"
     variation       3726
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199727314"
     variation       3732
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201182907"
     variation       3733
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:201608046"
     variation       3775
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:56732269"
     variation       3782..3785
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="ctct"
                     /db_xref="dbSNP:25610"
     variation       3803
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370901394"
     variation       3855
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375596683"
     variation       3871..3872
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="acta"
                     /db_xref="dbSNP:375689381"
     variation       3901
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:181335402"
     variation       3970
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:117188261"
     variation       3987
                     /gene="CTNNA2"
                     /gene_synonym="CAP-R; CAPR; CT114; CTNR"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:202190228"
ORIGIN      
ctagcggcgatccgggccgctgccgctcgcgcttgggcaggacgcggggcgggcggggggaggggggagcggcttcgcttccagccccgagtgaggcggagacccaggcgggcgggcagagcaggcggcaccgcacctcggccagaggcggctgcagcagctgctgcccttgtccctgccgccgcctctccagtcccttctgtgattaccactccagctgctgggaacgggcgagaaagaggaggaggcgagaaactcccaccgacccacagagggagcatgacttcggcaacttcacctatcattctgaaatgggaccccaaaagtttggaaatccggacgctaacagtggaaaggctgttggagccacttgttacacaggtgactacacttgtcaacacaagcaacaaaggcccatctggtaaaaagaaagggaggtcaaagaaagcccatgtactagctgcctctgtagagcaagccactcagaatttcctggaaaagggtgaacagatcgctaaggagagtcaagatctcaaagaagagttggtggctgctgtagaggatgtgcgcaaacaaggtgagacgatgcggatcgcctcctccgagtttgcagatgacccttgctcgtcggtaaagcgcggcaccatggtacgggcggcaagggctttgctctccgcggtgacacgcttactcatcctggcggacatggcagatgtcatgagacttttatcccatctgaaaattgtggaagaggccctggaagctgtcaaaaatgctacaaatgagcaagaccttgcaaaccgttttaaagagtttgggaaagagatggtgaaacttaactatgtagcagcaagaagacaacaggagctgaaggatcctcactgtcgggatgagatggcagccgcccgaggggctctgaagaagaatgccacaatgctgtacacggcctctcaagcatttctccgccacccagatgtcgccgctacgagagccaaccgagattatgtgttcaaacaagtccaggaggccatcgccggcatctccaatgctgctcaagctacctcgcccactgacgaagccaagggccacacgggcatcggcgagctggctgcggctcttaatgagtttgacaataagattatcctggaccccatgacgttcagcgaggccaggttccggccgtccctggaggagaggctggagagcatcatcagcggcgcagcgctgatggccgactcctcctgcacgcgagacgaccggcgcgagaggatcgtggcggagtgcaacgccgtgcggcaggcgctccaggacctgctcagcgagtacatgaataatactggaaggaaagaaaaaggagatcctctcaacattgcgattgataagatgactaagaaaacaagagatctaaggagacagcttcggaaagcagtgatggatcacatatctgactctttcctggaaaccaatgttcctttgctagttctcattgaggctgcaaagagcggaaatgaaaaggaagtgaaagaatatgcccaagttttccgtgagcatgccaacaaactggtagaggttgccaatttggcctgttccatctccaacaatgaagaaggggtgaaattagttcggatggcagccacccagattgacagcctgtgtccccaggtcatcaatgccgctctgacactggctgcccggccacagagcaaagttgctcaggataacatggacgtcttcaaagaccagtgggagaagcaggtccgagtgttgacagaggccgtggatgacatcacctcagtggatgacttcctctctgtctcagaaaatcacatcttggaggatgtgaacaagtgtgtgatagccctccaagagggcgatgtggacactctggaccggactgcaggggccatcaggggccgggcagctcgagtcatacacatcatcaatgctgagatggagaactatgaagctggggtttatactgagaaggtgttggaagctacaaaattgctttctgaaacagtgatgccacgcttcgctgaacaagtagaggttgccattgaagccctgagtgccaacgttcctcaaccgtttgaggagaatgagttcatcgatgcctctcgcctggtgtatgatggcgttcgggacatcagaaaggctgtgctgatgatcaggaccccagaagaactagaggatgattctgactttgagcaggaagattatgatgtgcgtagcaggacaagtgttcagactgaggatgaccagctcattgcagggcagagcgcacgggccatcatggcgcaactaccgcaggaggagaaggcaaaaatagctgagcaggtggagatattccatcaagagaaaagcaagctggatgcagaagtggccaaatgggacgacagcggcaatgatatcattgtactggccaagcagatgtgtatgatcatgatggaaatgacagacttcacaagaggcaaaggcccattgaaaaatacatctgatgtcattaatgctgccaagaaaattgccgaagcaggttctcgaatggacaaattagctcgtgctgtggctgatcagtgtcctgattcagcatgtaagcaggatttattagcctaccttcaacgaattgccttgtattgccatcagcttaatatctgcagcaaggtgaaggcagaagtgcagaatctgggaggagagctcattgtgtcagggctggacagtgccacatcgcttatccaggcagctaaaaacctgatgaatgctgttgtcctcacggtgaaagcatcctatgtggcctcaaccaaataccagaaggtctatgggacagcagctgtcaactcacctgttgtgtcttggaagatgaaggctccagagaagaagccccttgtgaagagagaaaagcctgaagaattccagacacgagttcgacgaggttctcagaagaaacacatttcgcctgtacaggctttaagtgaattcaaagcaatggattccttctaggacgataggttttaacaagaaagctttttctttcttttctttctttctttttctttttaattccatttttgtatgcatacctgccagctcgtatgcctctggcatggggaaattaagggaacagtgtctgtttgcatgtaagatgagatgagatcaatactactgatccatctgtagcctgggaaggagacaggacattcctgtactaaggtggcacagagctgtcctttgcaacattctcataaaattgggcacagagttcgcattggcgcaatatttatgggagtgggagggatggggaaaataaacttaactctacaaaagcaaactctaatgcatgcaagaatcattaggttggcaggtatatgcataagtgaaaaatctggaagtgtaatggtagaacataaaacttgtattgcttctgtttcagtgcaaaaatgtactagccaatacgcttaagtgtgtggcccatgaattgaacaatttaaccttgaagtctatatccgtgatattatgtcgatttttaactgaggggaaattaactagtccagcctaaaatgcttcttttaatctgcattctgtttcctcttctagttgtgccattactagtgatcatgtttttttcccccctttaatgaaaacaataaacatctatttgagacaattaaaatccttctgggggcactggaagcacaatacggtgaccaatcttgctttcatttttttttctttttaatttgaaccatgattttgctagaaatagaaggcccagtggtggaatattagagggaaggaaactgacaacgtgtgaaagttagaggcaaatacataggtgtagcttggagtgctggtatctaatataccattgtattcactaactaactcaaaataaacacatttaatcttgacatctcaagtatgttttcttttttaattttttaagtatgtacttaataaagattagagcatcatcttcctgaaaattcattaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:1496 -> Molecular function: GO:0005200 [structural constituent of cytoskeleton] evidence: NAS
            GeneID:1496 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:1496 -> Molecular function: GO:0045296 [cadherin binding] evidence: IEA
            GeneID:1496 -> Biological process: GO:0007409 [axonogenesis] evidence: ISS
            GeneID:1496 -> Biological process: GO:0016337 [cell-cell adhesion] evidence: ISS
            GeneID:1496 -> Biological process: GO:0021942 [radial glia guided migration of Purkinje cell] evidence: ISS
            GeneID:1496 -> Biological process: GO:0042692 [muscle cell differentiation] evidence: TAS
            GeneID:1496 -> Biological process: GO:0048813 [dendrite morphogenesis] evidence: ISS
            GeneID:1496 -> Biological process: GO:0048854 [brain morphogenesis] evidence: ISS
            GeneID:1496 -> Biological process: GO:0051149 [positive regulation of muscle cell differentiation] evidence: TAS
            GeneID:1496 -> Biological process: GO:0051823 [regulation of synapse structural plasticity] evidence: ISS
            GeneID:1496 -> Biological process: GO:0060134 [prepulse inhibition] evidence: ISS
            GeneID:1496 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
            GeneID:1496 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
            GeneID:1496 -> Cellular component: GO:0005912 [adherens junction] evidence: ISS
            GeneID:1496 -> Cellular component: GO:0005913 [cell-cell adherens junction] evidence: IEA
            GeneID:1496 -> Cellular component: GO:0015629 [actin cytoskeleton] evidence: IEA
            GeneID:1496 -> Cellular component: GO:0016323 [basolateral plasma membrane] evidence: IEA
            GeneID:1496 -> Cellular component: GO:0030027 [lamellipodium] evidence: IEA
            GeneID:1496 -> Cellular component: GO:0030424 [axon] evidence: ISS

by @meso_cacase at DBCLS
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