Type | Description |
---|---|
Definition | ess-2 splicing factor homolog |
Date | Results | Publications |
---|---|---|
2018-04-07 10:55:00 | Experiments using Ess2 deletion mutants showed that a C-terminus deletion mutant of Ess2 (1-399 a. a.) lost its ability to associate with snRNAs, whereas the N-terminus domain of Ess2 (1-200 a. a.) associated with retinoic acid receptor-related orphan receptor gamma/gamma-t, but not with snRNAs. | 29454968 |
2010-09-15 22:06:00 | Observational study of gene-disease association. (HuGE Navigator) | 19913121 |
2008-03-13 08:46:00 | Observational study of gene-disease association. (HuGE Navigator) | 16432632 |
Type | IDs |
---|---|
Synonymous | DGCR13, DGCR14, DGS-H, DGS-I, DGSH, DGSI, ES2, ESS-2, Es2el, bis1 |
Gene |
UniProtKB-ID:
ESS2_HUMAN,
F8WEF8_HUMAN
UniprotKB:
Q96DF8,
F8WEF8
UniParc:
UPI0000D4E27C,
UPI0000129227
EMBL:
BC006542,
L78010,
BC003015,
CR456344,
AC004471
Ensembl:
ENSG00000100056
KO:
hsa:8220
|
Nucleutide sequences |
EMBL-CDS:
AAL40039.1,
CAG30230.1,
AAH06542.1,
AAH03015.1
Ensembl_TRS:
ENST00000252137,
ENST00000434568
|
Protein sequencees |
Ensembl_PRO:
ENSP00000252137,
ENSP00000388524
RefSeq:
XP_016884447.1,
XP_006724392.1,
XP_005261339.1,
XP_006724393.1,
XP_016884448.1,
XP_006724394.1,
XP_011528705.1,
XP_011528706.1,
NP_073210.1
|
Others |
UniRef100:
UniRef100_Q96DF8,
UniRef100_F8WEF8
UniRef90:
UniRef90_Q96DF8,
UniRef90_F8WEF8
UniRef50:
UniRef50_F8WEF8,
UniRef50_Q96DF8
UniGene:
Hs.517407,
Hs.741535
CCDS:
CCDS13756.1
|
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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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