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63977 PRDM15

63977

PRDM15

PR/SET domain 15

protein-coding

Homo sapiens

基因描述

Type Description
Definition PR/SET domain 15

研究结论

Date Results Publications
2020-09-19 16:26:00 PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly. 31950080
2017-10-28 13:15:00 Findings indicate that PR domain containing 15 protein (PRDM15) is important in both mouse and human induced pluripotent stem cells (iPSCs) reprogramming. 28740264

名称对应

Type IDs
Synonymous C21orf83, PFM15, ZNF298
Gene
UniProtKB-ID: PRD15_HUMAN, E7ER26_HUMAN
UniprotKB: P57071, E7ER26
UniParc: UPI0000456FFA, UPI000290A521, UPI000198C844, UPI000047F44C, UPI000198C843, UPI0000D74C4C
EMBL: AY063456, AB051814, AP001745, AB051812, AB126081, AP001619, KF495739, AEKP01110574, AP002955, AF276513, AP001618, AP001580, CH471079, AF426259, AB051813, AB051815, AF426260, AY078498, AMYH02037867
Ensembl: ENSG00000141956
KO: hsa:63977
Nucleutide sequences
EMBL-CDS: BAA95527.1, EAX09585.1, AAM53516.1, AAL60596.1, BAD99020.1, BAD99015.1, AAL85487.2, BAD99017.1, AAF78093.1, BAD99018.1, AAM53515.1, BAD99016.1
Ensembl_TRS: ENST00000433067, ENST00000449395, ENST00000422911, ENST00000398548, ENST00000269844, ENST00000447016
Protein sequencees
Ensembl_PRO: ENSP00000381556, ENSP00000415471, ENSP00000269844, ENSP00000396943, ENSP00000408592, ENSP00000431410
RefSeq: XP_011527978.1, XP_011527983.1, XP_006724103.1, NP_071398.5, NP_001269863.2, NP_001035514.2, XP_011527977.1, XP_011527976.1, XP_011527980.1, XP_016883915.1, XP_011527985.1, XP_011527979.1, XP_006724102.1, XP_016883914.1, XP_011527981.1
Others
UniRef100: UniRef100_P57071, UniRef100_E7ER26
UniRef90: UniRef90_P57071, UniRef90_E7ER26
UniRef50: UniRef50_M3WHE7, UniRef50_P57071
UniGene: Hs.473893, Hs.726680

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