| Type | Description |
|---|---|
| Definition | TATA-box binding protein associated factor 2 |
| Date | Results | Publications |
|---|---|---|
| 2016-02-13 11:48:00 | the TAF2-TAF8-TAF10 complex demonstrates that there is a stepwise assembly pathway of nuclear holo-TFIID, regulated by nuclear import of preformed cytoplasmic submodules | 25586196 |
| 2014-07-12 10:52:00 | This study suggested that the Microcephaly thin corpus callosum intellectual disability syndrome is caused by the more conserved mutation p.Thr186Arg, with the second sequence change identified, p.Pro416His. | 24084144 |
| Type | IDs |
|---|---|
| Synonymous | CIF150, MRT40, TAF2B, TAFII150 |
| Gene |
UniProtKB-ID:
TAF2_HUMAN,
B3KMD8_HUMAN,
A0A024R9E6_HUMAN
UniprotKB:
Q6P1X5,
B3KMD8,
A0A024R9E6
UniParc:
UPI0000210507,
UPI000015F36F,
UPI0000EE32B0
EMBL:
AK001618,
BC047732,
AF026445,
CH471060,
AK316592,
AF040701,
BC064830,
AF057694,
AC107960,
BC035673,
AC021945
Ensembl:
ENSG00000064313
KO:
hsa:6873
|
| Nucleutide sequences |
EMBL-CDS:
AAC13540.1,
AAH35673.1,
BAG38179.1,
AAC68502.1,
AAH64830.1,
AAC02966.1,
AAH47732.1,
BAG50950.1,
EAW91992.1,
EAW91991.1,
EAW91993.1
Gene_ORFName:
hCG_19954
Ensembl_TRS:
ENST00000378164
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000367406
RefSeq:
XP_016869268.1,
XP_016869280.1,
XP_006716684.1,
XP_016869270.1,
XP_016869274.1,
XP_024303008.1,
XP_011515561.1,
XP_016869269.1,
XP_016869271.1,
XP_024303010.1,
NP_003175.2,
XP_024303009.1,
XP_024303011.1,
XP_016869275.1,
XP_016869279.1,
XP_016869272.1
|
| Others |
UniRef100:
UniRef100_Q6P1X5,
UniRef100_B3KMD8
UniRef90:
UniRef90_Q6P1X5,
UniRef90_B3KMD8
UniRef50:
UniRef50_Q6P1X5,
UniRef50_B3KMD8
UniGene:
Hs.122752
CCDS:
CCDS34937.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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