Home |
Help |
Advanced search
2024-04-20 14:16:18, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_016428 2129 bp mRNA linear PRI 15-JUN-2013
DEFINITION Homo sapiens ABI family, member 3 (ABI3), transcript variant 1,
mRNA.
ACCESSION NM_016428
VERSION NM_016428.2 GI:29337288
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 2129)
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 2 (bases 1 to 2129)
AUTHORS Latini,F.R., Hemerly,J.P., Freitas,B.C., Oler,G., Riggins,G.J. and
Cerutti,J.M.
TITLE ABI3 ectopic expression reduces in vitro and in vivo cell growth
properties while inducing senescence
JOURNAL BMC Cancer 11, 11 (2011)
PUBMED 21223585
REMARK GeneRIF: Result links ABI3 to the pathogenesis and progression of
some cancers and suggests that ABI3 or its pathway might have
interest as therapeutic target.
Publication Status: Online-Only
REFERENCE 3 (bases 1 to 2129)
AUTHORS Venkatesan,K., Rual,J.F., Vazquez,A., Stelzl,U., Lemmens,I.,
Hirozane-Kishikawa,T., Hao,T., Zenkner,M., Xin,X., Goh,K.I.,
Yildirim,M.A., Simonis,N., Heinzmann,K., Gebreab,F., Sahalie,J.M.,
Cevik,S., Simon,C., de Smet,A.S., Dann,E., Smolyar,A.,
Vinayagam,A., Yu,H., Szeto,D., Borick,H., Dricot,A., Klitgord,N.,
Murray,R.R., Lin,C., Lalowski,M., Timm,J., Rau,K., Boone,C.,
Braun,P., Cusick,M.E., Roth,F.P., Hill,D.E., Tavernier,J.,
Wanker,E.E., Barabasi,A.L. and Vidal,M.
TITLE An empirical framework for binary interactome mapping
JOURNAL Nat. Methods 6 (1), 83-90 (2009)
PUBMED 19060904
REFERENCE 4 (bases 1 to 2129)
AUTHORS Hirao,N., Sato,S., Gotoh,T., Maruoka,M., Suzuki,J., Matsuda,S.,
Shishido,T. and Tani,K.
TITLE NESH (Abi-3) is present in the Abi/WAVE complex but does not
promote c-Abl-mediated phosphorylation
JOURNAL FEBS Lett. 580 (27), 6464-6470 (2006)
PUBMED 17101133
REMARK GeneRIF: NESH (Abi-3), like Abi-1 and Abi-2, is a component of the
Abi/WAVE complex, but likely plays a different role in the
regulation of c-Abl.
REFERENCE 5 (bases 1 to 2129)
AUTHORS Ichigotani,Y., Fujii,K., Hamaguchi,M. and Matsuda,S.
TITLE In search of a function for the E3B1/Abi2/Argbp1/NESH family
(Review)
JOURNAL Int. J. Mol. Med. 9 (6), 591-595 (2002)
PUBMED 12011975
REMARK Review article
REFERENCE 6 (bases 1 to 2129)
AUTHORS Ichigotani,Y., Yokozaki,S., Fukuda,Y., Hamaguchi,M. and Matsuda,S.
TITLE Forced expression of NESH suppresses motility and metastatic
dissemination of malignant cells
JOURNAL Cancer Res. 62 (8), 2215-2219 (2002)
PUBMED 11956071
REMARK GeneRIF: Forced expression of NESH suppresses motility and
metastatic dissemination of malignant cells.
REFERENCE 7 (bases 1 to 2129)
AUTHORS Matsuda,S., Iriyama,C., Yokozaki,S., Ichigotani,Y., Shirafuji,N.,
Yamaki,K., Hayakawa,T. and Hamaguchi,M.
TITLE Cloning and sequencing of a novel human gene that encodes a
putative target protein of Nesh-SH3
JOURNAL J. Hum. Genet. 46 (8), 483-486 (2001)
PUBMED 11501947
REFERENCE 8 (bases 1 to 2129)
AUTHORS Miyazaki,K., Matsuda,S., Ichigotani,Y., Takenouchi,Y., Hayashi,K.,
Fukuda,Y., Nimura,Y. and Hamaguchi,M.
TITLE Isolation and characterization of a novel human gene (NESH) which
encodes a putative signaling molecule similar to e3B1 protein
JOURNAL Biochim. Biophys. Acta 1493 (1-2), 237-241 (2000)
PUBMED 10978530
REFERENCE 9 (bases 1 to 2129)
AUTHORS Simpson,J.C., Wellenreuther,R., Poustka,A., Pepperkok,R. and
Wiemann,S.
TITLE Systematic subcellular localization of novel proteins identified by
large-scale cDNA sequencing
JOURNAL EMBO Rep. 1 (3), 287-292 (2000)
PUBMED 11256614
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AB037886.1.
On Mar 28, 2003 this sequence version replaced gi:7705980.
Summary: This gene encodes a member of an adaptor protein family.
Members of this family encode proteins containing a homeobox
homology domain, proline rich region and Src-homology 3 (SH3)
domain, and are components of the Abi/WAVE complex which regulates
Rac-dependent actin polymerization. The encoded protein inhibits
ectopic metastasis of tumor cells as well as cell migration. This
may be accomplished through interaction with p21-activated kinase.
[provided by RefSeq, Sep 2008].
Transcript Variant: This variant (1) represents the longer
transcript and encodes the longer isoform (1).
##Evidence-Data-START##
Transcript exon combination :: AB037886.1, AL136709.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025085, ERS025086 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
FEATURES Location/Qualifiers
source 1..2129
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="17"
/map="17q21.3"
gene 1..2129
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/note="ABI family, member 3"
/db_xref="GeneID:51225"
/db_xref="HGNC:29859"
/db_xref="HPRD:05900"
/db_xref="MIM:606363"
exon 1..615
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/inference="alignment:Splign:1.39.8"
variation 63
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2233364"
misc_feature 94..96
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/note="upstream in-frame stop codon"
variation 94
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:149838793"
variation 107
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:12948271"
variation 250..261
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace=""
/replace="tgggcccccaaa"
/db_xref="dbSNP:140527653"
variation 344
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:73338394"
variation 387
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:188837768"
variation 388
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:377689573"
variation 445
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:192806498"
variation 464
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2233365"
CDS 499..1599
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/note="isoform 1 is encoded by transcript variant 1; ABI
gene family, member 3; new molecule including SH3; ABI
gene family member 3"
/codon_start=1
/product="ABI gene family member 3 isoform 1"
/protein_id="NP_057512.1"
/db_xref="GI:7705981"
/db_xref="CCDS:CCDS11546.1"
/db_xref="GeneID:51225"
/db_xref="HGNC:29859"
/db_xref="HPRD:05900"
/db_xref="MIM:606363"
/translation="
MAELQQLQEFEIPTGREALRGNHSALLRVADYCEDNYVQATDKRKALEETMAFTTQALASVAYQVGNLAGHTLRMLDLQGAALRQVEARVSTLGQMVNMHMEKVARREIGTLATVQRLPPGQKVIAPENLPPLTPYCRRPLNFGCLDDIGHGIKDLSTQLSRTGTLSRKSIKAPATPASATLGRPPRIPEPVHLPVVPDGRLSAASSASSLASAGSAEGVGGAPTPKGQAAPPAPPLPSSLDPPPPPAAVEVFQRPPTLEELSPPPPDEELPLPLDLPPPPPLDGDELGLPPPPPGFGPDEPSWVPASYLEKVVTLYPYTSQKDNELSFSEGTVICVTRRYSDGWCEGVSSEGTGFFPGNYVEPSC
"
misc_feature 775..996
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/note="Abl-interactor HHR; Region: Abi_HHR; pfam07815"
/db_xref="CDD:149081"
misc_feature 1432..1587
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/note="Src homology 3 domain of Abl Interactor proteins;
Region: SH3_Abi; cd11826"
/db_xref="CDD:212760"
misc_feature order(1447..1449,1453..1455,1462..1464,1474..1476,
1528..1533,1570..1572,1576..1581)
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/note="peptide ligand binding site [polypeptide binding];
other site"
/db_xref="CDD:212760"
variation 511
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:143414853"
variation 544
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:370923583"
variation 564
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:376299895"
variation 574
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:201115503"
variation 598
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:146754613"
exon 616..783
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/inference="alignment:Splign:1.39.8"
variation 628
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:200790496"
variation 629
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:2233369"
variation 635
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:143540619"
variation 649
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:143614623"
variation 652
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200111501"
variation 707
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:371444697"
variation 723
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201757928"
variation 742
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:374915787"
variation 755
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:199999962"
variation 759
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:35031462"
variation 763
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:369657954"
exon 784..960
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/inference="alignment:Splign:1.39.8"
variation 788
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:202087269"
variation 794
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:377358127"
variation 813
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:145273532"
variation 831
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:117896869"
variation 838
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:187673177"
variation 841
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:201557264"
variation 845
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:142527437"
variation 848
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:137924898"
variation 868
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:139297199"
variation 955
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:370412209"
exon 961..1046
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/inference="alignment:Splign:1.39.8"
variation 990
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:73340306"
variation 1020
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:2233371"
exon 1047..1142
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/inference="alignment:Splign:1.39.8"
variation 1121
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:199635084"
variation 1124
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:616338"
exon 1143..1300
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/inference="alignment:Splign:1.39.8"
variation 1143
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:147987389"
variation 1149
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:76617033"
variation 1159
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200867869"
variation 1164
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:376591517"
variation 1174
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:150532080"
variation 1180
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:369790283"
variation 1210
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139539456"
variation 1217
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368043560"
variation 1229
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:371508417"
variation 1248
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:375202610"
variation 1269
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:141746983"
exon 1301..1435
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/inference="alignment:Splign:1.39.8"
variation 1302
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:146244763"
variation 1303
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200803220"
variation 1326
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:371106947"
variation 1336
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:139368451"
variation 1342
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:144160707"
variation 1349
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="t"
/db_xref="dbSNP:145120343"
variation 1357
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:199538050"
variation 1417
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:373253578"
variation 1426
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:377169529"
variation 1428
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:370459926"
exon 1436..2109
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/inference="alignment:Splign:1.39.8"
variation 1441
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:150100821"
variation 1452
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:142832429"
variation 1514
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:201030368"
variation 1524
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:151062169"
variation 1542
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:368794979"
variation 1543
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:200202572"
variation 1603
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:2233374"
variation 1624
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="g"
/replace="t"
/db_xref="dbSNP:368644987"
variation 1634
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:371956623"
variation 1918
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:114842800"
variation 1921
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="g"
/db_xref="dbSNP:187442799"
variation 1946
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="c"
/db_xref="dbSNP:191319602"
variation 1991..1992
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace=""
/replace="c"
/db_xref="dbSNP:34526681"
variation 1993
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:183237512"
variation 1995
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="c"
/replace="t"
/db_xref="dbSNP:11545136"
variation 2077
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/replace="a"
/replace="g"
/db_xref="dbSNP:56327802"
polyA_site 2109
/gene="ABI3"
/gene_synonym="NESH; SSH3BP3"
/experiment="experimental evidence, no additional details
recorded"
ORIGIN
tcctatccaccctccactcccctgtcccttggtgactcatccctgagcttcccaaggaagcccccaccctctgccctttcctcccgccttccatgagtggaaaatccacctccgccccctatagcaggccagcccccttcctccccagtctccgaccccatcccccagccgaccagtttcctctccaggaccagggagcaatcacagctgccccgaccttggcttcctctgctgggtgggattgggggctgggcccccaaatgggcccctggcttcccccttcctctgggcaggggacagagagacacaggctcggggagcaggactgacttcctcttgtcccggaatgagcatgcctgccctttgcaagcaggtttgggtctcacgcagaggaaaccaaaagcaataagagggagggaaggcagagcaaccaatcaagggcagggtgagactcaaaacgagcgggctccctggggagccagacagaggctgggggtgatggcggagctacagcagctgcaggagtttgagatccccactggccgggaggctctgaggggcaaccacagtgccctgctgcgggtcgctgactactgcgaggacaactatgtgcaggccacagacaagcggaaggcgctggaggagaccatggccttcactacccaggcactggccagcgtggcctaccaggtgggcaacctggccgggcacactctgcgcatgttggacctgcagggggccgccctgcggcaggtggaagcccgtgtaagcacgctgggccagatggtgaacatgcatatggagaaggtggcccgaagggagatcggcaccttagccactgtccagcggctgccccccggccagaaggtcatcgccccagagaacctaccccctctcacgccctactgcaggagacccctcaactttggctgcctggacgacattggccatgggatcaaggacctcagcacgcagctgtcaagaacaggcaccctgtctcgaaagagcatcaaggcccctgccacacccgcctccgccaccttggggagaccaccccggattcccgagccagtgcacctgccggtggtgcccgacggcagactctccgccgcctcctctgcgtcttccctggcctcggccggcagcgccgaaggtgtcggtggggcccccacgcccaaggggcaggcagcacctccagccccacctctccccagctccttggacccacctcctccaccagcagccgtcgaggtgttccagcggcctcccacgctggaggagttgtccccacccccaccggacgaagagctgcccctgccactggacctgcctcctcctccacccctggatggagatgaattggggctgcctccacccccaccaggatttgggcctgatgagcccagctgggtgcctgcctcatacttggagaaagtggtgacactgtacccatacaccagccagaaggacaatgagctctccttctctgagggcactgtcatctgtgtcactcgccgctactccgatggctggtgcgagggcgtcagctcagaggggactggattcttccctgggaactatgtggagcccagctgctgacagcccagggctctctgggcagctgatgtctgcactgagtgggtttcatgagccccaagccaaaaccagctccagtcacagctggactgggtctgcccacctcttgggctgtgagctgtgttctgtccttcctcccatcggagggagaaggggtcctggggagagagaatttatccagaggcctgctgcagatggggaagagctggaaaccaagaagtttgtcaacagaggacccctactccatgcaggacagggtctcctgctgcaagtcccaactttgaataaaacagatgatgtcctgtgactgccccacagagataaggggccaggagggattgaaaggcatcccagttctaaggctgctgctaattacagcccccaacctccaacccaccagctgacctagaagcagcatcttcccatttcctcagtacccacaaagtgcagcccacattggaccccagacacccctctgcagccattgactgcaacttgttcttttgcccattgaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:51225 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:51225 -> Biological process: GO:0006928 [cellular component movement] evidence: NAS
GeneID:51225 -> Biological process: GO:0018108 [peptidyl-tyrosine phosphorylation] evidence: IDA
GeneID:51225 -> Biological process: GO:0030334 [regulation of cell migration] evidence: IDA
GeneID:51225 -> Cellular component: GO:0005622 [intracellular] evidence: IDA
GeneID:51225 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:51225 -> Cellular component: GO:0005737 [cytoplasm] evidence: NAS
GeneID:51225 -> Cellular component: GO:0030027 [lamellipodium] evidence: IDA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.