Type | Description |
---|---|
Definition | PR/SET domain 15 |
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 |
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
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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