Type | Description |
---|---|
Definition | PR domain containing 13 |
Date | Results | Publications |
---|---|---|
2018-05-19 11:24:00 | The findings highlight the function of PRDM13 in repressing the activity of basic helix-loop-helix transcriptional activators that together are required to achieve precise neuronal specification during mouse development. | 28850031 |
2018-03-31 11:28:00 | data show that Prdm13 is not required for amacrine fate as a class, but is essential for the formation of Ebf3+ amacrine cell subtypes. Rather than driving subtype identity, Prdm13 may act by restricting competing fate programs to maintain identity and survival. | 29258872 |
2015-12-19 11:41:00 | Findings indicate that Prdm13/Nkx2-1-mediated signaling in the DMC declines with advanced age, leading to decreased sleep quality and increased adiposity. | 25546159 |
2015-08-08 11:39:00 | Targeted deletion of Prdm13 leads to a specific reduction of amacrine cells and changes visual sensitivity. | 25995483 |
Type | IDs |
---|---|
Gene |
UniProtKB-ID:
PRD13_MOUSE
UniprotKB:
E9PZZ1
UniParc:
UPI00003568EE,
UPI00001E35ED
EMBL:
AL672159
Ensembl:
ENSMUSG00000040478
KO:
mmu:230025
|
Nucleutide sequences |
Ensembl_TRS:
ENSMUST00000076206,
ENSMUST00000095141
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000092761,
ENSMUSP00000075562
RefSeq:
NP_001074240.1,
XP_006537870.1,
XP_006537869.1
|
Others |
UniRef100:
UniRef100_E9PZZ1
UniRef90:
UniRef90_E9PZZ1
UniRef50:
UniRef50_E9PZZ1
UniGene:
Mm.208541
CCDS:
CCDS38699.1
|
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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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