Type | Description |
---|---|
Definition | zinc finger HIT-type containing 3 |
Date | Results | Publications |
---|---|---|
2017-11-04 12:00:00 | results suggest that loss-of-function missense mutation of znhit3 underlies PEHO syndrome. | 28335020 |
2017-05-07 01:43:00 | Results solve the structure of a complex resulting from interaction between protein fragments of human NUFIP1 and its cofactor ZNHIT3, and emphasize their imbrication. Also, it seems that the complexes involving NUFIP1, ZNHIT3, and SNU13 share strong structural similarities between human and yeast, suggesting that the initial steps of the box C/D snoRNP assembly process are conserved among species. | 27594683 |
2010-01-25 11:58:00 | Results identify TRIP3 as a novel regulator of PPARgamma-mediated adipocyte differentiation. | 19596656 |
2010-01-21 00:00:00 | A high GYPC gene expression is associated with an unfavorable outcome, in contrast, a high TRIP3 gene expression is associated with a favorable outcome in childhood ALL. | 19149918 |
Type | IDs |
---|---|
Synonymous | PEHO, TRIP3 |
Gene |
UniProtKB-ID:
ZNHI3_HUMAN,
A0A024R0X8_HUMAN
UniprotKB:
Q15649,
A0A024R0X8
UniParc:
UPI0000072634,
UPI0000E59F29
EMBL:
L40410,
CH471199,
BC017931,
AC126327,
AF400652,
AK290858
Ensembl:
ENSG00000273611,
ENSG00000278574
KO:
hsa:9326
|
Nucleutide sequences |
EMBL-CDS:
BAF83547.1,
AAH17931.1,
AAM82423.1,
EAW57552.1,
AAC41737.1,
EAW57554.1
Gene_ORFName:
hCG_30201
Ensembl_TRS:
ENST00000620508,
ENST00000619649,
ENST00000617429,
ENST00000620324
|
Protein sequencees |
Ensembl_PRO:
ENSP00000479727,
ENSP00000484687,
ENSP00000481504,
ENSP00000478183
RefSeq:
NP_001268363.1,
NP_001268361.1,
NP_001268362.1,
NP_004764.1
|
Others |
UniRef100:
UniRef100_Q15649
UniRef90:
UniRef90_Q15649
UniRef50:
UniRef50_Q15649
UniGene:
Hs.2210
CCDS:
CCDS62156.1,
CCDS11312.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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