2025-05-09 19:27:35, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_002202 2729 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens ISL LIM homeobox 1 (ISL1), mRNA. ACCESSION NM_002202 VERSION NM_002202.2 GI:115387113 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 2729) AUTHORS Graham,R.P., Shrestha,B., Caron,B.L., Smyrk,T.C., Grogg,K.L., Lloyd,R.V. and Zhang,L. TITLE Islet-1 is a sensitive but not entirely specific marker for pancreatic neuroendocrine neoplasms and their metastases JOURNAL Am. J. Surg. Pathol. 37 (3), 399-405 (2013) PUBMED 23348208 REMARK GeneRIF: Our findings confirm that Isl1 is a sensitive marker of pancreatic origin in cases of metastatic neuroendocrine neoplasms . REFERENCE 2 (bases 1 to 2729) AUTHORS Xue,L., Wang,X., Xu,J., Xu,X., Liu,X., Hu,Z., Shen,H. and Chen,Y. TITLE ISL1 common variant rs1017 is not associated with susceptibility to congenital heart disease in a Chinese population JOURNAL Genet Test Mol Biomarkers 16 (7), 679-683 (2012) PUBMED 22480195 REMARK GeneRIF: This is the first study which indicates that ISL1 common variant rs1017 may not play a role in sporadic CHD susceptibility in the Chinese population. REFERENCE 3 (bases 1 to 2729) AUTHORS Koo,J., Mertens,R.B., Mirocha,J.M., Wang,H.L. and Dhall,D. TITLE Value of Islet 1 and PAX8 in identifying metastatic neuroendocrine tumors of pancreatic origin JOURNAL Mod. Pathol. 25 (6), 893-901 (2012) PUBMED 22388755 REMARK GeneRIF: Both Islet 1 and PAX8 are reliable immunohistochemical markers for identifying metastatic neuroendocrine tumors of pancreatic origin. REFERENCE 4 (bases 1 to 2729) AUTHORS Wang,X., Shaffer,J.R., Zeng,Z., Begum,F., Vieira,A.R., Noel,J., Anjomshoaa,I., Cuenco,K.T., Lee,M.K., Beck,J., Boerwinkle,E., Cornelis,M.C., Hu,F.B., Crosslin,D.R., Laurie,C.C., Nelson,S.C., Doheny,K.F., Pugh,E.W., Polk,D.E., Weyant,R.J., Crout,R., McNeil,D.W., Weeks,D.E., Feingold,E. and Marazita,M.L. TITLE Genome-wide association scan of dental caries in the permanent dentition JOURNAL BMC Oral Health 12, 57 (2012) PUBMED 23259602 REMARK Publication Status: Online-Only REFERENCE 5 (bases 1 to 2729) AUTHORS Golzio,C., Havis,E., Daubas,P., Nuel,G., Babarit,C., Munnich,A., Vekemans,M., Zaffran,S., Lyonnet,S. and Etchevers,H.C. TITLE ISL1 directly regulates FGF10 transcription during human cardiac outflow formation JOURNAL PLoS ONE 7 (1), E30677 (2012) PUBMED 22303449 REMARK GeneRIF: The relationship between human ISL1 and FGF10 within the embryonic time window during which the linear heart tube remodels into four chambers, was examined. REFERENCE 6 (bases 1 to 2729) AUTHORS Pfaff,S.L., Mendelsohn,M., Stewart,C.L., Edlund,T. and Jessell,T.M. TITLE Requirement for LIM homeobox gene Isl1 in motor neuron generation reveals a motor neuron-dependent step in interneuron differentiation JOURNAL Cell 84 (2), 309-320 (1996) PUBMED 8565076 REFERENCE 7 (bases 1 to 2729) AUTHORS Riggs,A.C., Tanizawa,Y., Aoki,M., Wasson,J., Ferrer,J., Rabin,D.U., Vaxillaire,M., Froguel,P. and Permutt,M.A. TITLE Characterization of the LIM/homeodomain gene islet-1 and single nucleotide screening in NIDDM JOURNAL Diabetes 44 (6), 689-694 (1995) PUBMED 7789634 REFERENCE 8 (bases 1 to 2729) AUTHORS Tanizawa,Y., Riggs,A.C., Dagogo-Jack,S., Vaxillaire,M., Froguel,P., Liu,L., Donis-Keller,H. and Permutt,M.A. TITLE Isolation of the human LIM/homeodomain gene islet-1 and identification of a simple sequence repeat polymorphism [corrected] JOURNAL Diabetes 43 (7), 935-941 (1994) PUBMED 7912209 REMARK Erratum:[Diabetes 1994 Sep;43(9):1171] REFERENCE 9 (bases 1 to 2729) AUTHORS Wang,M. and Drucker,D.J. TITLE The LIM domain homeobox gene isl-1: conservation of human, hamster, and rat complementary deoxyribonucleic acid sequences and expression in cell types of nonneuroendocrine lineage JOURNAL Endocrinology 134 (3), 1416-1422 (1994) PUBMED 7907017 REFERENCE 10 (bases 1 to 2729) AUTHORS Dong,J., Asa,S.L. and Drucker,D.J. TITLE Islet cell and extrapancreatic expression of the LIM domain homeobox gene isl-1 JOURNAL Mol. Endocrinol. 5 (11), 1633-1641 (1991) PUBMED 1685766 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010478.5, BC031213.1, BC017027.1 and BM680522.1. This sequence is a reference standard in the RefSeqGene project. On Sep 28, 2006 this sequence version replaced gi:4504736. Summary: This gene encodes a member of the LIM/homeodomain family of transcription factors. The encoded protein binds to the enhancer region of the insulin gene, among others, and may play an important role in regulating insulin gene expression. The encoded protein is central to the development of pancreatic cell lineages and may also be required for motor neuron generation. Mutations in this gene have been associated with maturity-onset diabetes of the young. [provided by RefSeq, Jul 2008]. 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 :: BC031213.1, U07559.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025090 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-576 AC010478.5 100186-100761 577-1026 BC031213.1 578-1027 1027-2448 BC017027.1 733-2154 2449-2729 BM680522.1 1-281 c FEATURES Location/Qualifiers source 1..2729 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="5" /map="5q11.1" gene 1..2729 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="ISL LIM homeobox 1" /db_xref="GeneID:3670" /db_xref="HGNC:6132" /db_xref="MIM:600366" exon 1..576 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /inference="alignment:Splign:1.39.8" variation 57 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:3762977" variation 67 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="g" /db_xref="dbSNP:71618117" variation 114 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:374921619" variation 124 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="g" /db_xref="dbSNP:377679399" variation 247 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:36216897" variation 309 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:116222082" variation 336 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:370591252" variation 340 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="g" /replace="t" /db_xref="dbSNP:375825065" variation 401 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:121913539" misc_feature 462..464 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="upstream in-frame stop codon" variation 502 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:3917084" variation 514 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="c" /db_xref="dbSNP:375345896" variation 528 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="c" /db_xref="dbSNP:372022305" variation 543 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:200164834" CDS 549..1598 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="ISL1 transcription factor, LIM/homeodomain; islet-1" /codon_start=1 /product="insulin gene enhancer protein ISL-1" /protein_id="NP_002193.2" /db_xref="GI:115387114" /db_xref="CCDS:CCDS43314.1" /db_xref="GeneID:3670" /db_xref="HGNC:6132" /db_xref="MIM:600366" /translation="
MGDMGDPPKKKRLISLCVGCGNQIHDQYILRVSPDLEWHAACLKCAECNQYLDESCTCFVRDGKTYCKRDYIRLYGIKCAKCSIGFSKNDFVMRARSKVYHIECFRCVACSRQLIPGDEFALREDGLFCRADHDVVERASLGAGDPLSPLHPARPLQMAAEPISARQPALRPHVHKQPEKTTRVRTVLNEKQLHTLRTCYAANPRPDALMKEQLVEMTGLSPRVIRVWFQNKRCKDKKRSIMMKQLQQQQPNDKTNIQGMTGTPMVAASPERHDGGLQANPVEVQSYQPPWKVLSDFALQSDIDQPAFQQLVNFSEGGPGSNSTGSEVASMSSQLPDTPNSMVASPIEA
" misc_feature 597..761 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="The first LIM domain of Isl, a member of LHX protein family; Region: LIM1_Isl; cd09366" /db_xref="CDD:188752" misc_feature order(597..599,606..608,663..665,672..674,681..683, 690..692,747..749,756..758) /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="Zn binding site [ion binding]; other site" /db_xref="CDD:188752" misc_feature 606..767 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="Region: LIM domain" misc_feature 783..947 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="The second LIM domain of Isl, a member of LHX protein family; Region: LIM2_Isl; cd09374" /db_xref="CDD:188760" misc_feature order(783..785,792..794,849..851,858..860,867..869, 876..878,933..935,942..944) /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="Zn binding site [ion binding]; other site" /db_xref="CDD:188760" misc_feature 792..956 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="Region: LIM domain" misc_feature 1095..1268 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="Homeodomain; DNA binding domains involved in the transcriptional regulation of key eukaryotic developmental processes; may bind to DNA as monomers or as homo- and/or heterodimers, in a sequence-specific manner; Region: homeodomain; cd00086" /db_xref="CDD:238039" misc_feature order(1095..1106,1110..1112,1161..1163,1179..1181, 1218..1220,1224..1229,1236..1241,1245..1253,1257..1262) /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:238039" misc_feature 1098..1277 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="Region: Homeodomain" misc_feature order(1098..1100,1107..1109,1227..1229,1236..1241, 1248..1250) /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /note="specific DNA base contacts [nucleotide binding]; other site" /db_xref="CDD:238039" misc_feature 1332..1421 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (P61371.1); Region: LIM-binding domain (LID) (By similarity)" variation 550 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:374259070" variation 570 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="g" /db_xref="dbSNP:368787467" exon 577..766 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /inference="alignment:Splign:1.39.8" variation 586 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="t" /db_xref="dbSNP:372177290" variation 587 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:189115217" variation 596 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:369145747" exon 767..1026 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /inference="alignment:Splign:1.39.8" STS 782..1235 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /standard_name="D10Bir8" /db_xref="UniSTS:141487" variation 798 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:373022588" variation 815 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="c" /db_xref="dbSNP:201853354" variation 824 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:376610562" variation 892 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:201797783" variation 977 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:374296284" variation 984 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="c" /db_xref="dbSNP:200172777" variation 985 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="g" /db_xref="dbSNP:371070257" variation 1006 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:374493957" variation 1007 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:368770808" exon 1027..1313 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /inference="alignment:Splign:1.39.8" variation 1052 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:2303751" variation 1053 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:375950160" variation 1061 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:121913540" variation 1089 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="t" /db_xref="dbSNP:200209474" variation 1115 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:121913541" variation 1154 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="t" /db_xref="dbSNP:200829118" variation 1170 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="g" /replace="t" /db_xref="dbSNP:376320342" variation 1263 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="c" /db_xref="dbSNP:199639357" variation 1303 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:121912286" exon 1314..1481 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /inference="alignment:Splign:1.39.8" variation 1326 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="t" /db_xref="dbSNP:371499581" variation 1367 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="g" /db_xref="dbSNP:373703337" variation 1371 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:371918442" variation 1433 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:41268419" variation 1434 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:372119962" exon 1482..2718 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /inference="alignment:Splign:1.39.8" variation 1533 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:199961324" variation 1586 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="c" /replace="t" /db_xref="dbSNP:201718508" variation 1602 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:369904787" variation 1628 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="g" /replace="t" /db_xref="dbSNP:183431669" variation 1638 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:374773039" variation 1681 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:139406174" STS 1810..2019 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /standard_name="D5S2482" /db_xref="UniSTS:181718" variation 1860..1861 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="" /replace="a" /db_xref="dbSNP:200597453" STS 1960..2710 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /standard_name="ISL1__6479" /db_xref="UniSTS:464505" variation 2033 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="c" /db_xref="dbSNP:201793590" variation 2113 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="g" /replace="t" /db_xref="dbSNP:1802593" variation 2135 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="g" /db_xref="dbSNP:370818896" variation 2137 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="g" /replace="t" /db_xref="dbSNP:41268421" STS 2143..2473 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /standard_name="D5S2482" /db_xref="UniSTS:69430" variation 2213 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="" /replace="t" /db_xref="dbSNP:35133332" variation 2237 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1006" variation 2249 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="a" /replace="t" /db_xref="dbSNP:1017" variation 2341 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="g" /replace="t" /db_xref="dbSNP:187027859" variation 2432..2433 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="" /replace="t" /replace="tt" /db_xref="dbSNP:3033046" variation 2601..2602 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" /replace="" /replace="c" /db_xref="dbSNP:35701884" polyA_signal 2688..2693 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" polyA_site 2714 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" polyA_site 2718 /gene="ISL1" /gene_synonym="Isl-1; ISLET1" ORIGIN
gaaggaagaggaagaggaggagagggaggccagagccagaacagcccggcagcccgagcttcgggggagaacggcctgagccccgagcaagttgcctcgggagccctaatcctctcccgctggctcgccgagcggtcagtggcgctcagcggcggcgaggctgaaatatgataatcagaacagctgcgccgcgcgccctgcagccaatgggcgcggcgctcgcctgacgtccccgcgcgctgcgtcagaccaatggcgatggagctgagttggagcagagaagtttgagtaagagataaggaagagaggtgcccgagccgcgccgagtctgccgccgccgcagcgcctccgctccgccaactccgccggcttaaattggactcctagatccgcgagggcgcggcgcagccgagcagcggctctttcagcattggcaaccccaggggccaatatttcccacttagccacagctccagcatcctctctgtgggctgttcaccaactgtacaaccaccatttcactgtggacattactccctcttacagatatgggagacatgggagatccaccaaaaaaaaaacgtctgatttccctatgtgttggttgcggcaatcagattcacgatcagtatattctgagggtttctccggatttggaatggcatgcggcatgtttgaaatgtgcggagtgtaatcagtatttggacgagagctgtacatgctttgttagggatgggaaaacctactgtaaaagagattatatcaggttgtacgggatcaaatgcgccaagtgcagcatcggcttcagcaagaacgacttcgtgatgcgtgcccgctccaaggtgtatcacatcgagtgtttccgctgtgtggcctgcagccgccagctcatccctggggacgaatttgcgcttcgggaggacggtctcttctgccgagcagaccacgatgtggtggagagggccagtctaggcgctggcgacccgctcagtcccctgcatccagcgcggccactgcaaatggcagcggagcccatctccgccaggcagccagccctgcggccccacgtccacaagcagccggagaagaccacccgcgtgcggactgtgctgaacgagaagcagctgcacaccttgcggacctgctacgccgcaaacccgcggccagatgcgctcatgaaggagcaactggtagagatgacgggcctcagtccccgtgtgatccgggtctggtttcaaaacaagcggtgcaaggacaagaagcgaagcatcatgatgaagcaactccagcagcagcagcccaatgacaaaactaatatccaggggatgacaggaactcccatggtggctgccagtccagagagacacgacggtggcttacaggctaacccagtggaagtacaaagttaccagccaccttggaaagtactgagcgacttcgccttgcagagtgacatagatcagcctgcttttcagcaactggtcaatttttcagaaggaggaccgggctctaattccactggcagtgaagtagcatcaatgtcctctcaacttccagatacacctaacagcatggtagccagtcctattgaggcatgaggaacattcattctgtattttttttccctgttggagaaagtgggaaattataatgtcgaactctgaaacaaaagtatttaacgacccagtcaatgaaaactgaatcaagaaatgaatgctccatgaaatgcacgaagtctgttttaatgacaaggtgatatggtagcaacactgtgaagacaatcatgggattttactagaattaaacaacaaacaaaacgcaaaacccagtatatgctattcaatgatcttagaagtactgaaaaaaaaagacgtttttaaaacgtagaggatttatattcaaggatctcaaagaaagcattttcatttcactgcacatctagagaaaaacaaaaatagaaaattttctagtccatcctaatctgaatggtgctgtttctatattggtcattgccttgccaaacaggagctccagcaaaagcgcaggaagagagactggcctccttggctgaaagagtcctttcaggaaggtggagctgcattggtttgatatgtttaaagttgactttaacaaggggttaattgaaatcctgggtctcttggcctgtcctgtagctggtttattttttactttgccccctccccactttttttgagatccatcctttatcaagaagtctgaagcgactataaaggtttttgaattcagatttaaaaaccaacttataaagcattgcaacaaggttacctctattttgccacaagcgtctcgggattgtgtttgacttgtgtctgtccaagaacttttcccccaaagatgtgtatagttattggttaaaatgactgttttctctctctatggaaataaaaaggaaaaaaaaaaaggaaactttttttgtttgctcttgcattgcaaaaattataaagtaatttattatttattgtcggaagacttgccacttttcatgtcatttgacattttttgtttgctgaagtgaaaaaaaaagataaaggttgtacggtggtctttgaattatatgtctaattctatgtgttttgtctttttcttaaatattatgtgaaatcaaagcgccatatgtagaattatatcttcaggactatttcactaataaacatttggcatagataaataaataaaaaaaaaaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:3670 -> Molecular function: GO:0001102 [RNA polymerase II activating transcription factor binding] evidence: IPI GeneID:3670 -> Molecular function: GO:0001105 [RNA polymerase II transcription coactivator activity] evidence: IDA GeneID:3670 -> Molecular function: GO:0001158 [enhancer sequence-specific DNA binding] evidence: IDA GeneID:3670 -> Molecular function: GO:0001158 [enhancer sequence-specific DNA binding] evidence: NAS GeneID:3670 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA GeneID:3670 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:3670 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA GeneID:3670 -> Molecular function: GO:0016922 [ligand-dependent nuclear receptor binding] evidence: ISS GeneID:3670 -> Molecular function: GO:0030331 [estrogen receptor binding] evidence: ISS GeneID:3670 -> Molecular function: GO:0043425 [bHLH transcription factor binding] evidence: IPI GeneID:3670 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: ISS GeneID:3670 -> Biological process: GO:0001755 [neural crest cell migration] evidence: IEA GeneID:3670 -> Biological process: GO:0003139 [secondary heart field specification] evidence: IMP GeneID:3670 -> Biological process: GO:0003148 [outflow tract septum morphogenesis] evidence: ISS GeneID:3670 -> Biological process: GO:0003151 [outflow tract morphogenesis] evidence: ISS GeneID:3670 -> Biological process: GO:0003203 [endocardial cushion morphogenesis] evidence: ISS GeneID:3670 -> Biological process: GO:0003215 [cardiac right ventricle morphogenesis] evidence: ISS GeneID:3670 -> Biological process: GO:0003266 [regulation of secondary heart field cardioblast proliferation] evidence: IEA GeneID:3670 -> Biological process: GO:0008284 [positive regulation of cell proliferation] evidence: IEA GeneID:3670 -> Biological process: GO:0010575 [positive regulation vascular endothelial growth factor production] evidence: ISS GeneID:3670 -> Biological process: GO:0021520 [spinal cord motor neuron cell fate specification] evidence: IEA GeneID:3670 -> Biological process: GO:0021522 [spinal cord motor neuron differentiation] evidence: ISS GeneID:3670 -> Biological process: GO:0021524 [visceral motor neuron differentiation] evidence: IEA GeneID:3670 -> Biological process: GO:0021559 [trigeminal nerve development] evidence: ISS GeneID:3670 -> Biological process: GO:0021983 [pituitary gland development] evidence: IEA GeneID:3670 -> Biological process: GO:0031016 [pancreas development] evidence: ISS GeneID:3670 -> Biological process: GO:0031103 [axon regeneration] evidence: IEA GeneID:3670 -> Biological process: GO:0031290 [retinal ganglion cell axon guidance] evidence: IEA GeneID:3670 -> Biological process: GO:0032024 [positive regulation of insulin secretion] evidence: IC GeneID:3670 -> Biological process: GO:0032725 [positive regulation of granulocyte macrophage colony-stimulating factor production] evidence: ISS GeneID:3670 -> Biological process: GO:0032729 [positive regulation of interferon-gamma production] evidence: ISS GeneID:3670 -> Biological process: GO:0032730 [positive regulation of interleukin-1 alpha production] evidence: ISS GeneID:3670 -> Biological process: GO:0032731 [positive regulation of interleukin-1 beta production] evidence: ISS GeneID:3670 -> Biological process: GO:0032735 [positive regulation of interleukin-12 production] evidence: ISS GeneID:3670 -> Biological process: GO:0032755 [positive regulation of interleukin-6 production] evidence: ISS GeneID:3670 -> Biological process: GO:0032760 [positive regulation of tumor necrosis factor production] evidence: ISS GeneID:3670 -> Biological process: GO:0033147 [negative regulation of intracellular estrogen receptor signaling pathway] evidence: ISS GeneID:3670 -> Biological process: GO:0042517 [positive regulation of tyrosine phosphorylation of Stat3 protein] evidence: IEA GeneID:3670 -> Biological process: GO:0043388 [positive regulation of DNA binding] evidence: IEA GeneID:3670 -> Biological process: GO:0043524 [negative regulation of neuron apoptotic process] evidence: ISS GeneID:3670 -> Biological process: GO:0045665 [negative regulation of neuron differentiation] evidence: IEA GeneID:3670 -> Biological process: GO:0045766 [positive regulation of angiogenesis] evidence: ISS GeneID:3670 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: ISS GeneID:3670 -> Biological process: GO:0048665 [neuron fate specification] evidence: ISS GeneID:3670 -> Biological process: GO:0048762 [mesenchymal cell differentiation] evidence: ISS GeneID:3670 -> Biological process: GO:0048880 [sensory system development] evidence: ISS GeneID:3670 -> Biological process: GO:0048936 [peripheral nervous system neuron axonogenesis] evidence: ISS GeneID:3670 -> Biological process: GO:0050728 [negative regulation of inflammatory response] evidence: ISS GeneID:3670 -> Biological process: GO:0055010 [ventricular cardiac muscle tissue morphogenesis] evidence: ISS GeneID:3670 -> Biological process: GO:0060037 [pharyngeal system development] evidence: ISS GeneID:3670 -> Biological process: GO:0060379 [cardiac muscle cell myoblast differentiation] evidence: IEA GeneID:3670 -> Biological process: GO:0060384 [innervation] evidence: ISS GeneID:3670 -> Biological process: GO:0060413 [atrial septum morphogenesis] evidence: ISS GeneID:3670 -> Biological process: GO:0060913 [cardiac cell fate determination] evidence: IDA GeneID:3670 -> Biological process: GO:0071385 [cellular response to glucocorticoid stimulus] evidence: ISS GeneID:3670 -> Biological process: GO:0071657 [positive regulation of granulocyte colony-stimulating factor production] evidence: ISS GeneID:3670 -> Biological process: GO:0090074 [negative regulation of protein homodimerization activity] evidence: ISS GeneID:3670 -> Biological process: GO:0090090 [negative regulation of canonical Wnt receptor signaling pathway] evidence: IEA GeneID:3670 -> Biological process: GO:1901258 [positive regulation of macrophage colony-stimulating factor production] evidence: ISS GeneID:3670 -> Cellular component: GO:0005634 [nucleus] evidence: NAS GeneID:3670 -> Cellular component: GO:0005737 [cytoplasm] evidence: NAS
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