Type | Description |
---|---|
Definition | CECR2, histone acetyl-lysine reader |
Date | Results | Publications |
---|---|---|
2021-04-03 13:35:00 | Reported DNA repair protein CECR2, which is associated with neural tube defects in mice, is not required for double-strand break repair in primary neurospheres. | 32570002 |
2012-05-26 11:30:00 | Strain-specific modifier genes of Cecr2-associated exencephaly in mice. | 22045912 |
2012-03-24 11:13:00 | The results demonstrated a novel role of CECR2-containing complexes in spermatogenesis and showed that CECR2 interacts predominantly with SNF2H instead of SNF2L in the testis. | 22154806 |
2011-04-30 10:35:00 | Data show that two independent mutations of Cecr2 are also associated with specific inner ear defects. | 21246654 |
2011-01-01 10:10:00 | A novel Cecr2 null allele (Cecr2(tm1.1Hemc)) had a stronger penetrance of exencephaly than Cecr2(Gt45Bic) in both BALB/c and FVB/N strains, in addition to midline facial clefts and forebrain encephalocele in the FVB/N strain. | 20589882 |
Type | IDs |
---|---|
Synonymous | 2610101O16Rik, 2810409N01Rik, Gtl4 |
Gene |
UniProtKB-ID:
CECR2_MOUSE
UniprotKB:
E9Q2Z1
UniParc:
UPI00015AA3F2,
UPI00006053A1
EMBL:
AC135105,
AK129435,
AC084273,
BC060152
Ensembl:
ENSMUSG00000071226
KO:
mmu:330409
|
Nucleutide sequences |
EMBL-CDS:
AAH60152.1,
BAC98245.1
Ensembl_TRS:
ENSMUST00000100993,
ENSMUST00000112686
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000108306,
ENSMUSP00000098556
RefSeq:
XP_030111347.1,
XP_011239698.1,
XP_036022147.1,
XP_011239700.1,
XP_036022149.1,
NP_001121623.1,
XP_017177148.1,
XP_030111348.1,
NP_001355635.1,
XP_036022148.1,
XP_011239699.1
|
Others |
UniRef100:
UniRef100_E9Q2Z1
UniRef90:
UniRef90_E9Q2Z1
UniRef50:
UniRef50_E9Q2Z1
UniGene:
Mm.333357
CCDS:
CCDS51890.1,
CCDS90117.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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