2024-03-30 00:28:58, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001114978 4833 bp mRNA linear PRI 15-JUL-2013 DEFINITION Homo sapiens tumor protein p63 (TP63), transcript variant 2, mRNA. ACCESSION NM_001114978 VERSION NM_001114978.1 GI:169234656 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 4833) AUTHORS Montariello,D., Troiano,A., Malanga,M., Calabro,V. and Quesada,P. TITLE p63 involvement in poly(ADP-ribose) polymerase 1 signaling of topoisomerase I-dependent DNA damage in carcinoma cells JOURNAL Biochem. Pharmacol. 85 (7), 999-1006 (2013) PUBMED 23376119 REMARK GeneRIF: p63 Is a new player of the PARP1-dependent signalling of DNA damage REFERENCE 2 (bases 1 to 4833) AUTHORS Matin,R.N., Chikh,A., Chong,S.L., Mesher,D., Graf,M., Sanza',P., Senatore,V., Scatolini,M., Moretti,F., Leigh,I.M., Proby,C.M., Costanzo,A., Chiorino,G., Cerio,R., Harwood,C.A. and Bergamaschi,D. TITLE p63 is an alternative p53 repressor in melanoma that confers chemoresistance and a poor prognosis JOURNAL J. Exp. Med. 210 (3), 581-603 (2013) PUBMED 23420876 REMARK GeneRIF: data provide evidence of a physiological interaction between p63 with p53 whereby translocation of p63 to the mitochondria occurred through a codependent process with p53, whereas accumulation of p53 in the nucleus was prevented by p63 REFERENCE 3 (bases 1 to 4833) AUTHORS Ethayathulla,A.S., Nguyen,H.T. and Viadiu,H. TITLE Crystal structures of the DNA-binding domain tetramer of the p53 tumor suppressor family member p73 bound to different full-site response elements JOURNAL J. Biol. Chem. 288 (7), 4744-4754 (2013) PUBMED 23243311 REMARK GeneRIF: Crystal structures of the DNA-binding domain tetramer of the p53 tumor suppressor family member p73 bound to different full-site response elements REFERENCE 4 (bases 1 to 4833) AUTHORS Re,M., Magliulo,G., Ferrante,L., Zizzi,A., Santarelli,A., Stramazzotti,D., Lo Muzio,L., Goteri,G. and Rubini,C. TITLE p63 expression in laryngeal squamous cell carcinoma is related to tumor extension, histologic grade, lymph node involvement and clinical stage JOURNAL J. Biol. Regul. Homeost. Agents 27 (1), 121-129 (2013) PUBMED 23489692 REMARK GeneRIF: Abnormal expression of p63 may be involved in the early phases of laryngeal tumorigenesis. REFERENCE 5 (bases 1 to 4833) AUTHORS Yamaki,T., Suenaga,Y., Iuchi,T., Alagu,J., Takatori,A., Itami,M., Araki,A., Ohira,M., Inoue,M., Kageyama,H., Yokoi,S., Saeki,N. and Nakagawara,A. TITLE Temozolomide suppresses MYC via activation of TAp63 to inhibit progression of human glioblastoma JOURNAL Sci Rep 3, 1160 (2013) PUBMED 23362460 REMARK GeneRIF: Therefore, our results suggest that the TAp63-mediated transcriptional repression of MYC is a novel pathway regulating TMZ efficacy in GBM. REFERENCE 6 (bases 1 to 4833) AUTHORS Osada,M., Ohba,M., Kawahara,C., Ishioka,C., Kanamaru,R., Katoh,I., Ikawa,Y., Nimura,Y., Nakagawara,A., Obinata,M. and Ikawa,S. TITLE Cloning and functional analysis of human p51, which structurally and functionally resembles p53 JOURNAL Nat. Med. 4 (7), 839-843 (1998) PUBMED 9662378 REMARK Erratum:[Nat Med 1998 Sep;4(9):982] REFERENCE 7 (bases 1 to 4833) AUTHORS Trink,B., Okami,K., Wu,L., Sriuranpong,V., Jen,J. and Sidransky,D. TITLE A new human p53 homologue JOURNAL Nat. Med. 4 (7), 747-748 (1998) PUBMED 9662346 REMARK Erratum:[Nat Med 1998 Sep;4(9):982] REFERENCE 8 (bases 1 to 4833) AUTHORS Zeng,X., Levine,A.J. and Lu,H. TITLE Non-p53 p53RE binding protein, a human transcription factor functionally analogous to P53 JOURNAL Proc. Natl. Acad. Sci. U.S.A. 95 (12), 6681-6686 (1998) PUBMED 9618472 REFERENCE 9 (bases 1 to 4833) AUTHORS Bian,J. and Sun,Y. TITLE p53CP, a putative p53 competing protein that specifically binds to the consensus p53 DNA binding sites: a third member of the p53 family? JOURNAL Proc. Natl. Acad. Sci. U.S.A. 94 (26), 14753-14758 (1997) PUBMED 9405685 REFERENCE 10 (bases 1 to 4833) AUTHORS Robinson,A., Gibbins,J., Rodriguez-Linares,B., Finan,P.M., Wilson,L., Kellie,S., Findell,P. and Watson,S.P. TITLE Characterization of Grb2-binding proteins in human platelets activated by Fc gamma RIIA cross-linking JOURNAL Blood 88 (2), 522-530 (1996) PUBMED 8695800 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC078809.9, AC117486.3, AF075432.1, AC063939.15 and CB241431.1. Summary: This gene encodes a member of the p53 family of transcription factors. An animal model, p63 -/- mice, has been useful in defining the role this protein plays in the development and maintenance of stratified epithelial tissues. p63 -/- mice have several developmental defects which include the lack of limbs and other tissues, such as teeth and mammary glands, which develop as a result of interactions between mesenchyme and epithelium. Mutations in this gene are associated with ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3); split-hand/foot malformation 4 (SHFM4); ankyloblepharon-ectodermal defects-cleft lip/palate; ADULT syndrome (acro-dermato-ungual-lacrimal-tooth); limb-mammary syndrome; Rap-Hodgkin syndrome (RHS); and orofacial cleft 8. Both alternative splicing and the use of alternative promoters results in multiple transcript variants encoding different proteins. Many transcripts encoding different proteins have been reported but the biological validity and the full-length nature of these variants have not been determined. [provided by RefSeq, Jul 2008]. Transcript Variant: This variant (2) lacks an exon in the 3' coding region that results in a frameshift, compared to variant 1. The resulting protein (isoform 2, also known as TAp63beta) is shorter and has a distinct C-terminus, compared to isoform 1. 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## RNAseq introns :: single sample supports all introns ERS025084 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-151 AC078809.9 70492-70642 c 152-206 AC117486.3 43785-43839 c 207-1757 AF075432.1 1-1551 1758-4522 AC063939.15 114644-117408 4523-4833 CB241431.1 1-311 c FEATURES Location/Qualifiers source 1..4833 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="3" /map="3q28" gene 1..4833 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /note="tumor protein p63" /db_xref="GeneID:8626" /db_xref="HGNC:15979" /db_xref="MIM:603273" exon 1..151 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 4 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:147353819" variation 30 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:367604538" variation 32 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="t" /db_xref="dbSNP:28673064" misc_feature 66..68 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /note="upstream in-frame stop codon" variation 75 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:200935681" CDS 90..1757 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /note="isoform 2 is encoded by transcript variant 2; tumor protein p53-competing protein; tumor protein 63; amplified in squamous cell carcinoma; chronic ulcerative stomatitis protein; transformation-related protein 63; tumor protein p63 deltaN isoform delta; CUSP; keratinocyte transcription factor KET" /codon_start=1 /product="tumor protein 63 isoform 2" /protein_id="NP_001108450.1" /db_xref="GI:169234657" /db_xref="CCDS:CCDS46976.1" /db_xref="GeneID:8626" /db_xref="HGNC:15979" /db_xref="MIM:603273" /translation="
MNFETSRCATLQYCPDPYIQRFVETPAHFSWKESYYRSTMSQSTQTNEFLSPEVFQHIWDFLEQPICSVQPIDLNFVDEPSEDGATNKIEISMDCIRMQDSDLSDPMWPQYTNLGLLNSMDQQIQNGSSSTSPYNTDHAQNSVTAPSPYAQPSSTFDALSPSPAIPSNTDYPGPHSFDVSFQQSSTAKSATWTYSTELKKLYCQIAKTCPIQIKVMTPPPQGAVIRAMPVYKKAEHVTEVVKRCPNHELSREFNEGQIAPPSHLIRVEGNSHAQYVEDPITGRQSVLVPYEPPQVGTEFTTVLYNFMCNSSCVGGMNRRPILIIVTLETRDGQVLGRRCFEARICACPGRDRKADEDSIRKQQVSDSTKNGDGTKRPFRQNTHGIQMTSIKKRRSPDDELLYLPVRGRETYEMLLKIKESLELMQYLPQHTIETYRQQQQQQHQHLLQKQTSIQSPSSYGNSSPPLNKMNSMNKLPSVSQLINPQQRNALTPTTIPDGMGANIPMMGTHMPMAGDMNGLSPTQALPPPLSMPSTSHCTPPPPYPTDCSIVRIWQV
" misc_feature 90..410 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q9H3D4.1); Region: Transcription activation" misc_feature 618..1163 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /note="P53 DNA-binding domain; Region: P53; cd08367" /db_xref="CDD:176262" misc_feature order(819..821,828..830,1011..1013,1023..1025) /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /note="zinc binding site [ion binding]; other site" /db_xref="CDD:176262" misc_feature order(822..830,834..836) /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /note="dimerization site [polypeptide binding]; other site" /db_xref="CDD:176262" misc_feature order(1014..1016,1020..1022,1041..1043,1116..1118, 1122..1130,1137..1139) /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:176262" misc_feature 1143..1253 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q9H3D4.1); Region: Interaction with HIPK2" misc_feature 1263..1385 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /note="P53 tetramerisation motif; Region: P53_tetramer; pfam07710" /db_xref="CDD:149007" misc_feature 1269..1418 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q9H3D4.1); Region: Oligomerization" variation 108 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:376627647" variation 138 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:200000559" exon 152..280 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 156 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:144315591" variation 173 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="g" /replace="t" /db_xref="dbSNP:370716448" variation 198 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:147340040" variation 206 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:139505005" variation 266 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:151051217" exon 281..413 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 287 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="c" /db_xref="dbSNP:142452541" variation 293 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:376192818" variation 299 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:201631366" variation 344 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:368463552" variation 349 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="c" /db_xref="dbSNP:71308973" STS 364..435 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /standard_name="Trp63" /db_xref="UniSTS:526811" variation 375 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:372543100" variation 378 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:121908848" variation 392 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:186864205" exon 414..668 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 450 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:111466227" variation 455 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:201774402" variation 468 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:375508394" variation 475 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:193287780" variation 476 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:151335217" variation 488 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:145730343" variation 491 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:201239102" variation 521 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:200459305" variation 533 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:150028891" variation 587 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:146612442" variation 593 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:141278696" variation 607 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:113993965" variation 608 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:369833293" variation 610 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:201188464" variation 647 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:200355416" variation 656 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:373262255" exon 669..855 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 763 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:374833411" variation 766 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:193921145" STS 767..849 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /standard_name="PMC25851P1" /db_xref="UniSTS:272288" variation 767 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:61732782" variation 777 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:201466089" variation 786 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:121908838" variation 788 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:199727371" variation 800 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:199686014" variation 802 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:377757904" variation 814 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:201617537" variation 816 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:121908835" variation 817 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:121908836" variation 839 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:371524635" exon 856..971 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 886 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:121908849" variation 898 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="c" /db_xref="dbSNP:79939938" variation 928 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="t" /db_xref="dbSNP:190865056" variation 948 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:33979049" STS 970..1054 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /standard_name="PMC25851P2" /db_xref="UniSTS:272289" exon 972..1081 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 989 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:372807713" variation 1001 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:34119860" variation 1042 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:121908840" variation 1044 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:121908839" exon 1082..1218 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 1098 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:113993966" variation 1099 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:113993967" variation 1117 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:121908841" variation 1122 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:121908837" variation 1133 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:370101210" variation 1141 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:121908844" variation 1143 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:121908847" variation 1151 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:34841666" variation 1172 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:148937466" variation 1183 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:147148566" variation 1191 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:201706554" variation 1199 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:375593834" variation 1210 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:199807776" variation 1216 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:143591434" exon 1219..1301 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 1219 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:148052765" variation 1250 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:140374868" exon 1302..1438 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 1331 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:188455234" variation 1403 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:373897470" variation 1410 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:200973739" exon 1439..1596 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 1456 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:201479097" variation 1457 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:200558415" variation 1463 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:141794685" variation 1474 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:147181964" variation 1478 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="c" /db_xref="dbSNP:200802571" variation 1489 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:369453583" variation 1502 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:139407263" variation 1554 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:138832017" variation 1569 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:200203171" variation 1572 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:373849345" exon 1597..1741 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 1602 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:183154960" variation 1619 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="g" /replace="t" /db_xref="dbSNP:200578530" variation 1620 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="c" /db_xref="dbSNP:148076109" variation 1664 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:147389337" variation 1670 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:61752082" variation 1676 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:141847552" variation 1679 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:373284695" variation 1685 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:376238543" variation 1715 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:370637253" variation 1735 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:121908845" exon 1742..4815 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /inference="alignment:Splign:1.39.8" variation 1776 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:368336834" variation 1777 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="t" /db_xref="dbSNP:377605517" variation 1783 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:148577576" variation 1809 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:142981128" variation 1820 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:142762485" variation 1822 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:147538847" variation 1841 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="" /replace="c" /db_xref="dbSNP:113993964" variation 1872 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="g" /replace="t" /db_xref="dbSNP:372318389" variation 1902 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="c" /db_xref="dbSNP:376926686" variation 1943 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:140149400" variation 1950..1951 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="" /replace="t" /db_xref="dbSNP:35067146" variation 2000 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:143676789" variation 2001 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:369266838" variation 2016 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:34713855" variation 2029 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:140508531" variation 2054 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:201978861" variation 2083 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:34057105" variation 2115 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:140051057" variation 2411 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:188132962" variation 2417 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="t" /db_xref="dbSNP:192879052" variation 2473 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:78233713" variation 2509 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="t" /db_xref="dbSNP:144018872" variation 2579 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:73199799" variation 2665 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:184452906" variation 2676 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:6444406" variation 2892 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:187751631" variation 2935 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:35263259" variation 3015 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="t" /db_xref="dbSNP:192558999" variation 3211 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:184547631" variation 3299 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="g" /replace="t" /db_xref="dbSNP:201329652" variation 3381 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:35659283" variation 3424 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:35785527" variation 3464 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:36099321" variation 3475 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:370056499" variation 3510 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:375551286" variation 3559 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:181693641" variation 3589 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:373145775" variation 3638 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:35896507" variation 3658 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:34328757" variation 3793 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:185247541" variation 3816 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:189729625" variation 3824 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="" /replace="t" /db_xref="dbSNP:370280085" variation 3866 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:149875270" variation 3881..3882 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="" /replace="a" /db_xref="dbSNP:146332971" variation 3951 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:181220329" variation 3963 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /db_xref="dbSNP:144916141" variation 3977 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="" /replace="t" /db_xref="dbSNP:140654135" variation 3981 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:116568110" variation 4019 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:186045329" variation 4040 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="g" /replace="t" /db_xref="dbSNP:35969817" variation 4054 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:115660354" variation 4061 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:189721510" variation 4161 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:36064124" variation 4177 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:35356690" variation 4188 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:181958566" variation 4254 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:35861864" variation 4270..4271 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="" /replace="g" /db_xref="dbSNP:35796357" variation 4322 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:146760848" variation 4356 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="g" /db_xref="dbSNP:199834330" variation 4383 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:35592567" variation 4515 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="g" /replace="t" /db_xref="dbSNP:186295449" STS 4533..4728 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /standard_name="WI-11062" /db_xref="UniSTS:31046" variation 4576 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="" /replace="t" /db_xref="dbSNP:201395656" variation 4663 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="a" /replace="t" /db_xref="dbSNP:35694511" variation 4674 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="" /replace="a" /db_xref="dbSNP:5855278" variation 4724 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" /replace="c" /replace="t" /db_xref="dbSNP:151060923" polyA_signal 4793..4798 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" polyA_site 4815 /gene="TP63" /gene_synonym="AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L" ORIGIN
cccggctttatatctatatatacacaggtatatgtgtatattttatataattgttctccgttcgttgatatcaaagacagttgaaggaaatgaattttgaaacttcacggtgtgccaccctacagtactgccctgacccttacatccagcgtttcgtagaaaccccagctcatttctcttggaaagaaagttattaccgatccaccatgtcccagagcacacagacaaatgaattcctcagtccagaggttttccagcatatctgggattttctggaacagcctatatgttcagttcagcccattgacttgaactttgtggatgaaccatcagaagatggtgcgacaaacaagattgagattagcatggactgtatccgcatgcaggactcggacctgagtgaccccatgtggccacagtacacgaacctggggctcctgaacagcatggaccagcagattcagaacggctcctcgtccaccagtccctataacacagaccacgcgcagaacagcgtcacggcgccctcgccctacgcacagcccagctccaccttcgatgctctctctccatcacccgccatcccctccaacaccgactacccaggcccgcacagtttcgacgtgtccttccagcagtcgagcaccgccaagtcggccacctggacgtattccactgaactgaagaaactctactgccaaattgcaaagacatgccccatccagatcaaggtgatgaccccacctcctcagggagctgttatccgcgccatgcctgtctacaaaaaagctgagcacgtcacggaggtggtgaagcggtgccccaaccatgagctgagccgtgaattcaacgagggacagattgcccctcctagtcatttgattcgagtagaggggaacagccatgcccagtatgtagaagatcccatcacaggaagacagagtgtgctggtaccttatgagccaccccaggttggcactgaattcacgacagtcttgtacaatttcatgtgtaacagcagttgtgttggagggatgaaccgccgtccaattttaatcattgttactctggaaaccagagatgggcaagtcctgggccgacgctgctttgaggcccggatctgtgcttgcccaggaagagacaggaaggcggatgaagatagcatcagaaagcagcaagtttcggacagtacaaagaacggtgatggtacgaagcgcccgtttcgtcagaacacacatggtatccagatgacatccatcaagaaacgaagatccccagatgatgaactgttatacttaccagtgaggggccgtgagacttatgaaatgctgttgaagatcaaagagtccctggaactcatgcagtaccttcctcagcacacaattgaaacgtacaggcaacagcaacagcagcagcaccagcacttacttcagaaacagacctcaatacagtctccatcttcatatggtaacagctccccacctctgaacaaaatgaacagcatgaacaagctgccttctgtgagccagcttatcaaccctcagcagcgcaacgccctcactcctacaaccattcctgatggcatgggagccaacattcccatgatgggcacccacatgccaatggctggagacatgaatggactcagccccacccaggcactccctcccccactctccatgccatccacctcccactgcacacccccacctccgtatcccacagattgcagcattgtcaggatctggcaagtctgaaaatccctgagcaatttcgacatgcgatctggaagggcatcctggaccaccggcagctccacgaattctcctccccttctcatctcctgcggaccccaagcagtgcctctacagtcagtgtgggctccagtgagacccggggtgagcgtgttattgatgctgtgcgattcaccctccgccagaccatctctttcccaccccgagatgagtggaatgacttcaactttgacatggatgctcgccgcaataagcaacagcgcatcaaagaggagggggagtgagcctcaccatgtgagctcttcctatccctctcctaactgccagccccctaaaagcactcctgcttaatcttcaaagccttctccctagctcctccccttcctcttgtctgatttcttaggggaaggagaagtaagaggctacctcttacctaacatctgacctggcatctaattctgattctggctttaagccttcaaaactatagcttgcagaactgtagctgccatggctaggtagaagtgagcaaaaaagagttgggtgtctccttaagctgcagagatttctcattgacttttataaagcatgttcacccttatagtctaagactatatatataaatgtataaatatacagtatagatttttgggtggggggcattgagtattgtttaaaatgtaatttaaatgaaagaaaattgagttgcacttattgaccattttttaatttacttgttttggatggcttgtctatactccttcccttaaggggtatcatgtatggtgataggtatctagagcttaatgctacatgtgagtgacgatgatgtacagattctttcagttctttggattctaaatacatgccacatcaaacctttgagtagatccatttccattgcttattatgtaggtaagactgtagatatgtattcttttctcagtgttggtatattttatattactgacatttcttctagtgatgatggttcacgttggggtgatttaatccagttataagaagaagttcatgtccaaacgtcctctttagtttttggttgggaatgaggaaaattcttaaaaggcccatagcagccagttcaaaaacacccgacgtcatgtatttgagcatatcagtaacccccttaaatttaataccagataccttatcttacaatattgattgggaaaacatttgctgccattacagaggtattaaaactaaatttcactactagattgactaactcaaatacacatttgctactgttgtaagaattctgattgatttgattgggatgaatgccatctatctagttctaacagtgaagttttactgtctattaatattcagggtaaataggaatcattcagaaatgttgagtctgtactaaacagtaagatatctcaatgaaccataaattcaactttgtaaaaatcttttgaagcatagataatattgtttggtaaatgtttcttttgtttggtaaatgtttcttttaaagaccctcctattctataaaactctgcatgtagaggcttgtttacctttctctctctaaggtttacaataggagtggtgatttgaaaaatataaaattatgagattggttttcctgtggcataaattgcatcactgtatcattttcttttttaaccggtaagagtttcagtttgttggaaagtaactgtgagaacccagtttcccgtccatctcccttagggactacccatagacatgaaaggtccccacagagcaagagataagtctttcatggctgctgttgcttaaaccacttaaacgaagagttcccttgaaactttgggaaaacatgttaatgacaatattccagatctttcagaaatataacacatttttttgcatgcatgcaaatgagctctgaaatcttcccatgcattctggtcaagggctgtcattgcacataagcttccattttaattttaaagtgcaaaagggccagcgtggctctaaaaggtaatgtgtggattgcctctgaaaagtgtgtatatattttgtgtgaaattgcatactttgtattttgattattttttttttcttcttgggatagtgggatttccagaaccacacttgaaacctttttttatcgtttttgtattttcatgaaaataccatttagtaagaataccacatcaaataagaaataatgctacaattttaagaggggagggaagggaaagtttttttttattatttttttaaaattttgtatgttaaagagaatgagtccttgatttcaaagttttgttgtacttaaatggtaataagcactgtaaacttctgcaacaagcatgcagctttgcaaacccattaaggggaagaatgaaagctgttccttggtcctagtaagaagacaaactgcttcccttactttgctgagggtttgaataaacctaggacttccgagctatgtcagtactattcaggtaacactagggccttggaaattcctgtactgtgtctcatggatttggcactagccaaagcgaggcacccttactggcttacctcctcatggcagcctactctccttgagtgtatgagtagccagggtaaggggtaaaaggatagtaagcatagaaaccactagaaagtgggcttaatggagttcttgtggcctcagctcaatgcagttagctgaagaattgaaaagtttttgtttggagacgtttataaacagaaatggaaagcagagttttcattaaatccttttaccttttttttttcttggtaatcccctaaaataacagtatgtgggatattgaatgttaaagggatatttttttctattatttttataattgtacaaaattaagcaaatgttaaaagttttatatgctttattaatgttttcaaaaggtattatacatgtgatacattttttaagcttcagttgcttgtcttctggtactttctgttatgggcttttggggagccagaagccaatctacaatctctttttgtttgccaggacatgcaataaaatttaaaaaataaataaaaactaattaagaaattgaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:8626 -> Molecular function: GO:0001077 [RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription] evidence: IEA GeneID:8626 -> Molecular function: GO:0002039 [p53 binding] evidence: IBA GeneID:8626 -> Molecular function: GO:0003677 [DNA binding] evidence: NAS GeneID:8626 -> Molecular function: GO:0003682 [chromatin binding] evidence: IBA GeneID:8626 -> Molecular function: GO:0003682 [chromatin binding] evidence: IDA GeneID:8626 -> Molecular function: GO:0003684 [damaged DNA binding] evidence: IBA GeneID:8626 -> Molecular function: GO:0003690 [double-stranded DNA binding] evidence: IBA GeneID:8626 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IBA GeneID:8626 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:8626 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI GeneID:8626 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IBA GeneID:8626 -> Molecular function: GO:0044212 [transcription regulatory region DNA binding] evidence: IEA GeneID:8626 -> Molecular function: GO:0046872 [metal ion binding] evidence: IEA GeneID:8626 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IBA GeneID:8626 -> Biological process: GO:0001501 [skeletal system development] evidence: IEA GeneID:8626 -> Biological process: GO:0001736 [establishment of planar polarity] evidence: IEA GeneID:8626 -> Biological process: GO:0002053 [positive regulation of mesenchymal cell proliferation] evidence: IEA GeneID:8626 -> Biological process: GO:0002064 [epithelial cell development] evidence: IEA GeneID:8626 -> Biological process: GO:0006338 [chromatin remodeling] evidence: IEA GeneID:8626 -> Biological process: GO:0006915 [apoptotic process] evidence: IDA GeneID:8626 -> Biological process: GO:0006917 [induction of apoptosis] evidence: IEA GeneID:8626 -> Biological process: GO:0006978 [DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator] evidence: IBA GeneID:8626 -> Biological process: GO:0007219 [Notch signaling pathway] evidence: IEA GeneID:8626 -> Biological process: GO:0007499 [ectoderm and mesoderm interaction] evidence: IEA GeneID:8626 -> Biological process: GO:0007569 [cell aging] evidence: IEA GeneID:8626 -> Biological process: GO:0009954 [proximal/distal pattern formation] evidence: IEA GeneID:8626 -> Biological process: GO:0010165 [response to X-ray] evidence: IBA GeneID:8626 -> Biological process: GO:0010259 [multicellular organismal aging] evidence: IEA GeneID:8626 -> Biological process: GO:0010332 [response to gamma radiation] evidence: IBA GeneID:8626 -> Biological process: GO:0010481 [epidermal cell division] evidence: IEA GeneID:8626 -> Biological process: GO:0030216 [keratinocyte differentiation] evidence: IEA GeneID:8626 -> Biological process: GO:0030326 [embryonic limb morphogenesis] evidence: IEA GeneID:8626 -> Biological process: GO:0030859 [polarized epithelial cell differentiation] evidence: IEA GeneID:8626 -> Biological process: GO:0031069 [hair follicle morphogenesis] evidence: IEA GeneID:8626 -> Biological process: GO:0031571 [mitotic G1 DNA damage checkpoint] evidence: IBA GeneID:8626 -> Biological process: GO:0034644 [cellular response to UV] evidence: IBA GeneID:8626 -> Biological process: GO:0036342 [post-anal tail morphogenesis] evidence: IEA GeneID:8626 -> Biological process: GO:0042475 [odontogenesis of dentin-containing tooth] evidence: IEA GeneID:8626 -> Biological process: GO:0042771 [intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator] evidence: IBA GeneID:8626 -> Biological process: GO:0043066 [negative regulation of apoptotic process] evidence: IEA GeneID:8626 -> Biological process: GO:0043523 [regulation of neuron apoptotic process] evidence: IBA GeneID:8626 -> Biological process: GO:0043616 [keratinocyte proliferation] evidence: IEA GeneID:8626 -> Biological process: GO:0045617 [negative regulation of keratinocyte differentiation] evidence: IEA GeneID:8626 -> Biological process: GO:0045669 [positive regulation of osteoblast differentiation] evidence: IMP GeneID:8626 -> Biological process: GO:0045747 [positive regulation of Notch signaling pathway] evidence: IDA GeneID:8626 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IDA GeneID:8626 -> Biological process: GO:0045893 [positive regulation of transcription, DNA-dependent] evidence: IDA GeneID:8626 -> Biological process: GO:0045893 [positive regulation of transcription, DNA-dependent] evidence: NAS GeneID:8626 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IDA GeneID:8626 -> Biological process: GO:0048485 [sympathetic nervous system development] evidence: IEA GeneID:8626 -> Biological process: GO:0048745 [smooth muscle tissue development] evidence: IEA GeneID:8626 -> Biological process: GO:0048807 [female genitalia morphogenesis] evidence: IEA GeneID:8626 -> Biological process: GO:0051289 [protein homotetramerization] evidence: IPI GeneID:8626 -> Biological process: GO:0051402 [neuron apoptotic process] evidence: IEA GeneID:8626 -> Biological process: GO:0060157 [urinary bladder development] evidence: IEA GeneID:8626 -> Biological process: GO:0060197 [cloacal septation] evidence: IEA GeneID:8626 -> Biological process: GO:0060513 [prostatic bud formation] evidence: IEA GeneID:8626 -> Biological process: GO:0060529 [squamous basal epithelial stem cell differentiation involved in prostate gland acinus development] evidence: IEA GeneID:8626 -> Biological process: GO:2000381 [negative regulation of mesoderm development] evidence: IEA GeneID:8626 -> Cellular component: GO:0000785 [chromatin] evidence: IBA GeneID:8626 -> Cellular component: GO:0000790 [nuclear chromatin] evidence: IDA GeneID:8626 -> Cellular component: GO:0005634 [nucleus] evidence: IDA GeneID:8626 -> Cellular component: GO:0005634 [nucleus] evidence: NAS GeneID:8626 -> Cellular component: GO:0005654 [nucleoplasm] evidence: IDA GeneID:8626 -> Cellular component: GO:0005667 [transcription factor complex] evidence: IBA GeneID:8626 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA GeneID:8626 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA GeneID:8626 -> Cellular component: GO:0005794 [Golgi apparatus] evidence: IDA GeneID:8626 -> Cellular component: GO:0005829 [cytosol] evidence: IBA GeneID:8626 -> Cellular component: GO:0030425 [dendrite] evidence: IBA
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