Type | Description |
---|---|
Definition | PR domain containing 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, E130018M06Rik, ORF62, Zfp298 |
Gene |
UniProtKB-ID:
PRD15_MOUSE
UniprotKB:
E9Q8T2
UniParc:
UPI0001553856,
UPI00006078D5
EMBL:
AK144820,
AC121560
Ensembl:
ENSMUSG00000014039
KO:
mmu:114604
|
Nucleutide sequences |
EMBL-CDS:
BAE26081.1
Ensembl_TRS:
ENSMUST00000095849,
ENSMUST00000121584
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000113791,
ENSMUSP00000093533
RefSeq:
XP_030104791.1,
XP_030104793.1,
XP_030104792.1,
XP_006522928.1,
XP_006522932.1,
XP_006522929.1,
XP_036015638.1,
XP_006522933.1,
XP_030104790.1,
XP_030104789.1,
XP_006522931.1,
NP_659038.2,
NP_001346007.1,
XP_036015637.1,
NP_001346006.1,
XP_006522927.1,
XP_036015639.1
|
Others |
UniRef100:
UniRef100_E9Q8T2
UniRef90:
UniRef90_E9Q8T2
UniRef50:
UniRef50_E9Q8T2
UniGene:
Mm.328741
CCDS:
CCDS88979.1,
CCDS49926.1
|
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Refseq |
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Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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