2025-05-09 18:53:59, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_014112 9990 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens trichorhinophalangeal syndrome I (TRPS1), mRNA. ACCESSION NM_014112 VERSION NM_014112.2 GI:90652850 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 9990) AUTHORS Ripke S, Wray NR, Lewis CM, Hamilton SP, Weissman MM, Breen G, Byrne EM, Blackwood DH, Boomsma DI, Cichon S, Heath AC, Holsboer F, Lucae S, Madden PA, Martin NG, McGuffin P, Muglia P, Noethen MM, Penninx BP, Pergadia ML, Potash JB, Rietschel M, Lin D, Muller-Myhsok B, Shi J, Steinberg S, Grabe HJ, Lichtenstein P, Magnusson P, Perlis RH, Preisig M, Smoller JW, Stefansson K, Uher R, Kutalik Z, Tansey KE, Teumer A, Viktorin A, Barnes MR, Bettecken T, Binder EB, Breuer R, Castro VM, Churchill SE, Coryell WH, Craddock N, Craig IW, Czamara D, De Geus EJ, Degenhardt F, Farmer AE, Fava M, Frank J, Gainer VS, Gallagher PJ, Gordon SD, Goryachev S, Gross M, Guipponi M, Henders AK, Herms S, Hickie IB, Hoefels S, Hoogendijk W, Hottenga JJ, Iosifescu DV, Ising M, Jones I, Jones L, Jung-Ying T, Knowles JA, Kohane IS, Kohli MA, Korszun A, Landen M, Lawson WB, Lewis G, Macintyre D, Maier W, Mattheisen M, McGrath PJ, McIntosh A, McLean A, Middeldorp CM, Middleton L, Montgomery GM, Murphy SN, Nauck M, Nolen WA, Nyholt DR, O'Donovan M, Oskarsson H, Pedersen N, Scheftner WA, Schulz A, Schulze TG, Shyn SI, Sigurdsson E, Slager SL, Smit JH, Stefansson H, Steffens M, Thorgeirsson T, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, Volzke H, Weilburg JB, Willemsen G, Zitman FG, Neale B, Daly M, Levinson DF and Sullivan PF. CONSRTM Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium TITLE A mega-analysis of genome-wide association studies for major depressive disorder JOURNAL Mol. Psychiatry 18 (4), 497-511 (2013) PUBMED 22472876 REFERENCE 2 (bases 1 to 9990) AUTHORS Boraska,V., Davis,O.S., Cherkas,L.F., Helder,S.G., Harris,J., Krug,I., Liao,T.P., Treasure,J., Ntalla,I., Karhunen,L., Keski-Rahkonen,A., Christakopoulou,D., Raevuori,A., Shin,S.Y., Dedoussis,G.V., Kaprio,J., Soranzo,N., Spector,T.D., Collier,D.A. and Zeggini,E. TITLE Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits JOURNAL Am. J. Med. Genet. B Neuropsychiatr. Genet. 159B (7), 803-811 (2012) PUBMED 22911880 REFERENCE 3 (bases 1 to 9990) AUTHORS Divaris,K., Monda,K.L., North,K.E., Olshan,A.F., Lange,E.M., Moss,K., Barros,S.P., Beck,J.D. and Offenbacher,S. TITLE Genome-wide association study of periodontal pathogen colonization JOURNAL J. Dent. Res. 91 (7 SUPPL), 21S-28S (2012) PUBMED 22699663 REFERENCE 4 (bases 1 to 9990) AUTHORS Ackert-Bicknell,C.L., Demissie,S., Tsaih,S.W., Beamer,W.G., Cupples,L.A., Paigen,B.J., Hsu,Y.H., Kiel,D.P. and Karasik,D. TITLE Genetic variation in TRPS1 may regulate hip geometry as well as bone mineral density JOURNAL Bone 50 (5), 1188-1195 (2012) PUBMED 22306695 REMARK GeneRIF: Genetic variation in TRPS1 may regulate hip geometry as well as bone mineral density REFERENCE 5 (bases 1 to 9990) AUTHORS Sidler,J.A., Filges,I., Boesch,N., Ramelli,G.P., Rothlisberger,B., Huber,A.R., Tercanli,S., Bronz,L., Miny,P. and Heinimann,K. TITLE TRPS1 codon 952 constitutes a mutational hot spot in trichorhinophalangeal syndrome type I and could be associated with intellectual disability JOURNAL Clin. Dysmorphol. 21 (2), 87-90 (2012) PUBMED 22127049 REMARK GeneRIF: TRPS1 codon 952 constitutes a mutational hot spot in trichorhinophalangeal syndrome type I and could be associated with intellectual disability. REFERENCE 6 (bases 1 to 9990) AUTHORS Chang,G.T., Steenbeek,M., Schippers,E., Blok,L.J., van Weerden,W.M., van Alewijk,D.C., Eussen,B.H., van Steenbrugge,G.J. and Brinkmann,A.O. TITLE Characterization of a zinc-finger protein and its association with apoptosis in prostate cancer cells JOURNAL J. Natl. Cancer Inst. 92 (17), 1414-1421 (2000) PUBMED 10974077 REFERENCE 7 (bases 1 to 9990) AUTHORS Momeni,P., Glockner,G., Schmidt,O., von Holtum,D., Albrecht,B., Gillessen-Kaesbach,G., Hennekam,R., Meinecke,P., Zabel,B., Rosenthal,A., Horsthemke,B. and Ludecke,H.J. TITLE Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I JOURNAL Nat. Genet. 24 (1), 71-74 (2000) PUBMED 10615131 REFERENCE 8 (bases 1 to 9990) AUTHORS Ludecke,H.J., Schmidt,O., Nardmann,J., von Holtum,D., Meinecke,P., Muenke,M. and Horsthemke,B. TITLE Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8 JOURNAL Hum. Genet. 105 (6), 619-628 (1999) PUBMED 10647898 REFERENCE 9 (bases 1 to 9990) AUTHORS Hou,J., Parrish,J., Ludecke,H.J., Sapru,M., Wang,Y., Chen,W., Hill,A., Siegel-Bartelt,J., Northrup,H., Elder,F.F. et al. TITLE A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1) JOURNAL Genomics 29 (1), 87-97 (1995) PUBMED 8530105 REFERENCE 10 (bases 1 to 9990) AUTHORS Hamers,A., Jongbloet,P., Peeters,G., Fryns,J.P. and Geraedts,J. TITLE Severe mental retardation in a patient with tricho-rhino-phalangeal syndrome type I and 8q deletion JOURNAL Eur. J. Pediatr. 149 (9), 618-620 (1990) PUBMED 2373110 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AF183810.1, DA399687.1 and AF264784.1. This sequence is a reference standard in the RefSeqGene project. On Mar 28, 2006 this sequence version replaced gi:7657658. Summary: This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III. [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 :: AF183810.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025088 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-278 AF183810.1 28-305 279-319 DA399687.1 254-294 320-727 AF183810.1 341-748 728-5132 AF264784.1 296-4700 5133-9990 AF183810.1 5154-10011 FEATURES Location/Qualifiers source 1..9990 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="8" /map="8q24.12" gene 1..9990 /gene="TRPS1" /gene_synonym="GC79; LGCR" /note="trichorhinophalangeal syndrome I" /db_xref="GeneID:7227" /db_xref="HGNC:12340" /db_xref="MIM:604386" exon 1..457 /gene="TRPS1" /gene_synonym="GC79; LGCR" /inference="alignment:Splign:1.39.8" exon 458..615 /gene="TRPS1" /gene_synonym="GC79; LGCR" /inference="alignment:Splign:1.39.8" misc_feature 570..572 /gene="TRPS1" /gene_synonym="GC79; LGCR" /note="upstream in-frame stop codon" CDS 579..4463 /gene="TRPS1" /gene_synonym="GC79; LGCR" /note="zinc finger protein GC79; tricho-rhino-phalangeal syndrome type I protein" /codon_start=1 /product="zinc finger transcription factor Trps1" /protein_id="NP_054831.2" /db_xref="GI:90652851" /db_xref="CCDS:CCDS6318.2" /db_xref="GeneID:7227" /db_xref="HGNC:12340" /db_xref="MIM:604386" /translation="
MPYEVNAGYDFTNMVRKKNPPLRNVASEGEGQILEPIGTESKVSGKNKEFSADQMSENTDQSDAAELNHKEEHSLHVQDPSSSSKKDLKSAVLSEKAGFNYESPSKGGNFPSFPHDEVTDRNMLAFSSPAAGGVCEPLKSPQRAEADDPQDMACTPSGDSLETKEDQKMSPKATEETGQAQSGQANCQGLSPVSVASKNPQVPSDGGVRLNKSKTDLLVNDNPDPAPLSPELQDFKCNICGYGYYGNDPTDLIKHFRKYHLGLHNRTRQDAELDSKILALHNMVQFSHSKDFQKVNRSVFSGVLQDINSSRPVLLNGTYDVQVTSGGTFIGIGRKTPDCQGNTKYFRCKFCNFTYMGNSSTELEQHFLQTHPNKIKASLPSSEVAKPSEKNSNKSIPALQSSDSGDLGKWQDKITVKAGDDTPVGYSVPIKPLDSSRQNGTEATSYYWCKFCSFSCESSSSLKLLEHYGKQHGAVQSGGLNPELNDKLSRGSVINQNDLAKSSEGETMTKTDKSSSGAKKKDFSSKGAEDNMVTSYNCQFCDFRYSKSHGPDVIVVGPLLRHYQQLHNIHKCTIKHCPFCPRGLCSPEKHLGEITYPFACRKSNCSHCALLLLHLSPGAAGSSRVKHQCHQCSFTTPDVDVLLFHYESVHESQASDVKQEANHLQGSDGQQSVKESKEHSCTKCDFITQVEEEISRHYRRAHSCYKCRQCSFTAADTQSLLEHFNTVHCQEQDITTANGEEDGHAISTIKEEPKIDFRVYNLLTPDSKMGEPVSESVVKREKLEEKDGLKEKVWTESSSDDLRNVTWRGADILRGSPSYTQASLGLLTPVSGTQEQTKTLRDSPNVEAAHLARPIYGLAVETKGFLQGAPAGGEKSGALPQQYPASGENKSKDESQSLLRRRRGSGVFCANCLTTKTSLWRKNANGGYVCNACGLYQKLHSTPRPLNIIKQNNGEQIIRRRTRKRLNPEALQAEQLNKQQRGSNEEQVNGSPLERRSEDHLTESHQREIPLPSLSKYEAQGSLTKSHSAQQPVLVSQTLDIHKRMQPLHIQIKSPQESTGDPGNSSSVSEGKGSSERGSPIEKYMRPAKHPNYSPPGSPIEKYQYPLFGLPFVHNDFQSEADWLRFWSKYKLSVPGNPHYLSHVPGLPNPCQNYVPYPTFNLPPHFSAVGSDNDIPLDLAIKHSRPGPTANGASKEKTKAPPNVKNEGPLNVVKTEKVDRSTQDELSTKCVHCGIVFLDEVMYALHMSCHGDSGPFQCSICQHLCTDKYDFTTHIQRGLHRNNAQVEKNGKPKE
" misc_feature 996..998 /gene="TRPS1" /gene_synonym="GC79; LGCR" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 3291..3293 /gene="TRPS1" /gene_synonym="GC79; LGCR" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 3303..3458 /gene="TRPS1" /gene_synonym="GC79; LGCR" /note="Zinc finger DNA binding domain; binds specifically to DNA consensus sequence [AT]GATA[AG] promoter elements; a subset of family members may also bind protein; zinc-finger consensus topology is C-X(2)-C-X(17)-C-X(2)-C; Region: ZnF_GATA; cd00202" /db_xref="CDD:29259" misc_feature order(3303..3305,3312..3314,3366..3368,3375..3377) /gene="TRPS1" /gene_synonym="GC79; LGCR" /note="zinc binding site [ion binding]; other site" /db_xref="CDD:29259" misc_feature order(3330..3335,3339..3341,3366..3398,3447..3449, 3453..3458) /gene="TRPS1" /gene_synonym="GC79; LGCR" /note="DNA-binding region [nucleotide binding]; DNA binding site" /db_xref="CDD:29259" misc_feature 3855..3857 /gene="TRPS1" /gene_synonym="GC79; LGCR" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 3858..3860 /gene="TRPS1" /gene_synonym="GC79; LGCR" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" misc_feature 3870..3872 /gene="TRPS1" /gene_synonym="GC79; LGCR" /experiment="experimental evidence, no additional details recorded" /note="phosphorylation site" exon 616..1544 /gene="TRPS1" /gene_synonym="GC79; LGCR" /inference="alignment:Splign:1.39.8" exon 1545..2674 /gene="TRPS1" /gene_synonym="GC79; LGCR" /inference="alignment:Splign:1.39.8" exon 2675..3278 /gene="TRPS1" /gene_synonym="GC79; LGCR" /inference="alignment:Splign:1.39.8" exon 3279..3401 /gene="TRPS1" /gene_synonym="GC79; LGCR" /inference="alignment:Splign:1.39.8" exon 3402..9990 /gene="TRPS1" /gene_synonym="GC79; LGCR" /inference="alignment:Splign:1.39.8" STS 6553..6728 /gene="TRPS1" /gene_synonym="GC79; LGCR" /standard_name="A007K26" /db_xref="UniSTS:10749" STS 6594..6760 /gene="TRPS1" /gene_synonym="GC79; LGCR" /standard_name="RH16176" /db_xref="UniSTS:4640" variation 7226 /gene="TRPS1" /gene_synonym="GC79; LGCR" /replace="a" /replace="g" /db_xref="dbSNP:1661222" variation 7290 /gene="TRPS1" /gene_synonym="GC79; LGCR" /replace="a" /replace="g" /db_xref="dbSNP:800898" STS 7880..8707 /gene="TRPS1" /gene_synonym="GC79; LGCR" /standard_name="TRPS1__5142.2" /db_xref="UniSTS:468158" variation 8778 /gene="TRPS1" /gene_synonym="GC79; LGCR" /replace="g" /replace="t" /db_xref="dbSNP:800897" STS 9351..9513 /gene="TRPS1" /gene_synonym="GC79; LGCR" /standard_name="STS-H28054" /db_xref="UniSTS:7612" STS 9736..9906 /gene="TRPS1" /gene_synonym="GC79; LGCR" /standard_name="RH99133" /db_xref="UniSTS:84461" polyA_signal 9965..9970 /gene="TRPS1" /gene_synonym="GC79; LGCR" polyA_site 9988 /gene="TRPS1" /gene_synonym="GC79; LGCR" ORIGIN
aatagtgttggtgtcttgaaactgacgtaatgcgcggagactgaggtcctgacaagcgataacatttctgataaagacccgatcttactgcaatctctagcgtcctcttttttggtgctgctggtttctccagacctcgcgtcctctcgattgctctctcgccttcctatttcttttttttttttttaaacaaaaaacaacaccccctcccctctcccacccggcaccgggcacatccttgctctatttcctttctctttctctctctctctctctctctctcttttttaataagggtgggggagggaaaggggggggaggcaggaaagacctttttctctcccccccgcaataatccaagatcaactctgcaaacaacagaagacggttcatggctttggccgccgcgccaccatctttcgggctgccgagggtgttcttgacgattaatcaacagatgtacagatcagctctcaaaatgtcttctgtgtcttctgagcgtcttctaagacaattgcattagcctcctgctagttgactaatagaattaataattgtaaaaagcactctaaagccacatgccttatgaagtcaatgctgggtatgattttacaaatatggtccggaaaaagaacccccctctgagaaacgttgcaagtgaaggcgagggccagatcctggagcctataggtacagaaagcaaggtatctggaaagaacaaagaattttctgcagatcagatgtcagaaaatacggatcagagtgatgctgcagaactaaatcataaggaggaacatagcttgcatgttcaagatccatcttctagcagtaagaaggacttgaaaagcgcagttctgagtgagaaggctggcttcaattatgaaagccccagtaagggaggaaactttccctcctttccgcatgatgaggtgacagacagaaatatgttggctttctcatctccagctgctgggggagtctgtgagcccttgaagtctccgcaaagagcagaggcagatgaccctcaagatatggcctgcaccccctcaggggactcactggagacaaaggaagatcagaagatgtcaccaaaggctacagaggaaacagggcaagcacagagtggtcaagccaattgtcaaggtttgagcccagtttcagtggcctcaaaaaacccacaagtgccttcagatgggggtgtaagactgaataaatccaaaactgacttactggtgaatgacaacccagacccggcacctctgtctccagagcttcaggactttaaatgcaatatctgtggatatggttactacggcaacgaccccacagatctgattaagcacttccgaaagtatcacttaggactgcataaccgcaccaggcaagatgctgagctggacagcaaaatcttggcccttcataacatggtgcagttcagccattccaaagacttccagaaggtcaaccgttctgtgttttctggtgtgctgcaggacatcaattcttcaaggcctgttttactaaatgggacctatgatgtgcaggtgacttcaggtggaacattcattggcattggacggaaaacaccagattgccaagggaacaccaagtatttccgctgtaaattctgcaatttcacttatatgggcaactcatccaccgaattagaacaacattttcttcagactcacccaaacaaaataaaagcttctctcccctcctctgaggttgcaaaaccttcagagaaaaactctaacaagtccatccctgcacttcaatccagtgattctggagacttgggaaaatggcaggacaagataacagtcaaagcaggagatgacactcctgttgggtactcagtgcccataaagcccctcgattcctctagacaaaatggtacagaggccaccagttactactggtgtaaattttgtagtttcagctgtgagtcatctagctcacttaaactgctagaacattatggcaagcagcacggagcagtgcagtcaggcggccttaatccagagttaaatgataagctttccaggggctctgtcattaatcagaatgatctagccaaaagttcagaaggagagacaatgaccaagacagacaagagctcgagtggggctaaaaagaaggacttctccagcaagggagccgaggataatatggtaacgagctataattgtcagttctgtgacttccgatattccaaaagccatggccctgatgtaattgtagtggggccacttctccgtcattatcaacagctccataacattcacaagtgtaccattaaacactgtccattctgtcccagaggactttgcagcccagaaaagcaccttggagaaattacttatccgtttgcttgtagaaaaagtaattgttcccactgtgcactcttgcttctgcacttgtctcctggggcggctggaagctcgcgagtcaaacatcagtgccatcagtgttcattcaccacccctgacgtagatgtactcctctttcactatgaaagtgtgcatgagtcccaagcatcggatgtcaaacaagaagcaaatcacctgcaaggatcggatgggcagcagtctgtcaaggaaagcaaagaacactcatgtaccaaatgtgattttattacccaagtggaagaagagatttcccgacactacaggagagcacacagctgctacaaatgccgtcagtgcagttttacagctgccgatactcagtcactactggagcacttcaacactgttcactgccaggaacaggacatcactacagccaacggcgaagaggacggtcatgccatatccaccatcaaagaggagcccaaaattgacttcagggtctacaatctgctaactccagactctaaaatgggagagccagtttctgagagtgtggtgaagagagagaagctggaagagaaggacgggctcaaagagaaagtttggaccgagagttccagtgatgaccttcgcaatgtgacttggagaggggcagacatcctgcgggggagtccgtcatacacccaagcaagcctggggctgctgacgcctgtgtctggcacccaagagcagacaaagactctaagggatagtcccaatgtggaggccgcccatctggcgcgacctatttatggcttggctgtggaaaccaagggattcctgcagggggcgccagctggcggagagaagtctggggccctcccccagcagtatcctgcatcgggagaaaacaagtccaaggatgaatcccagtccctgttacggaggcgtagaggctccggtgttttttgtgccaattgcctgaccacaaagacctctctctggcgaaagaatgcaaatggcggatatgtatgcaacgcgtgtggcctctaccagaagcttcactcgactcccaggcctttaaacatcattaaacaaaacaacggtgagcagattattaggaggagaacaagaaagcgccttaacccagaggcacttcaggctgagcagctcaacaaacagcagaggggcagcaatgaggagcaagtcaatggaagcccgttagagaggaggtcagaagatcatctaactgaaagtcaccagagagaaattccactccccagcctaagtaaatacgaagcccagggttcattgactaaaagccattctgctcagcagccagtcctggtcagccaaactctggatattcacaaaaggatgcaacctttgcacattcagataaaaagtcctcaggaaagtactggagatccaggaaatagttcatccgtatctgaagggaaaggaagttctgagagaggcagtcctatagaaaagtacatgagacctgcgaaacacccaaattattcaccaccaggcagccctattgaaaagtaccagtacccactttttggacttccctttgtacataatgacttccagagtgaagctgattggctgcggttctggagtaaatataagctctccgttcctgggaatccgcactacttgagtcacgtgcctggcctaccaaatccttgccaaaactatgtgccttatcccaccttcaatctgcctcctcatttttcagctgttggatcagacaatgacattcctctagatttggcgatcaagcattccagacctgggccaactgcaaacggtgcctccaaggagaaaacgaaggcaccaccaaatgtaaaaaatgaaggtcccttgaatgtagtaaaaacagagaaagttgatagaagtactcaagatgaactttcaacaaaatgtgtgcactgtggcattgtctttctggatgaagtgatgtatgctttgcatatgagttgccatggtgacagtggacctttccagtgcagcatatgccagcatctttgcacggacaaatatgacttcacaacacatatccagaggggcctgcataggaacaatgcacaagtggaaaaaaatggaaaacctaaagagtaaaaccttagcacttagcacaattaaatagaaataggttttcttgatgggaattcaatagcttgtaatgtcttatgaagacctattaaaaaaatacttcatagagcctgccttatccaacatgaaattcccttcttttgttattctttcttttgatgagtaggttaccaagattaaaaagtgagataaatggtcaatgagaaagaatggaagatggtaaacaatcactttttaaaacctgttaagtcaaaaccatcttggctaatatgtactggggaaataatccataagagatatcaccagactagaattaatatatttataaagaaagagaccaaaactgtctagaatttgaaagggtttacatattattatactaaagcagtactggactggccattggaccatttgttccaaaacccataaattgttgcctaaatttataatgatcatgaaaccctaggcagaggaggagaaattgaaggtccagggcaatgaaagaaaaatggcgccctctcaatttagtcttctctcattggc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//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:7227 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:7227 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:7227 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA GeneID:7227 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA GeneID:7227 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IDA GeneID:7227 -> Biological process: GO:0001501 [skeletal system development] evidence: TAS GeneID:7227 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: TAS GeneID:7227 -> Biological process: GO:0006607 [NLS-bearing substrate import into nucleus] evidence: TAS GeneID:7227 -> Biological process: GO:0032330 [regulation of chondrocyte differentiation] evidence: ISS GeneID:7227 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
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