Type | Description |
---|---|
Definition | EGF domain specific O-linked N-acetylglucosamine transferase |
Date | Results | Publications |
---|---|---|
2021-04-17 13:15:00 | Bioinformatics and Functional Analyses Implicate Potential Roles for EOGT and L-fringe in Pancreatic Cancers. | 33562410 |
2018-02-17 10:47:00 | Analysis of midluteal endometrial biopsies revealed an inverse correlation between endometrial EOGT and ENHO expression and body mass index. obesity impairs the EOGT-adropin axis in decidual cells, which in turn points toward a mechanistic link between metabolic disorders and adverse pregnancy outcome. | 29244071 |
2017-12-16 10:19:00 | Eogt resulted in defective retinal angiogenesis, with a mild phenotype similar to that caused by reduced Notch signaling in retina. Combined deficiency of different Notch1 mutant alleles exacerbated the abnormalities in Eogt(-/-) retina, and Notch target gene expression was decreased in Eogt(-/-)endothelial cells. | 28395734 |
2017-05-06 10:59:00 | Studies provide evidence that mutations in EOGT lead to autosomal recessive Adams-Oliver Syndrome. [review] | 28408480 |
2014-10-11 12:26:00 | c.1074delA mutation segregates with Adams-Oliver syndrome in the Bedouin family. | 23860037 |
Type | IDs |
---|---|
Synonymous | AER61, AOS4, C3orf64, EOGT1 |
Gene |
UniProtKB-ID:
EOGT_HUMAN
UniprotKB:
Q5NDL2
UniParc:
UPI00002132FF,
UPI00015B3B86,
UPI00004982AF
EMBL:
BX640821,
BC060887,
AK290356,
KC347596,
AK294101,
AK126187,
AC109587,
AJ868234
Ensembl:
ENSG00000163378
KO:
hsa:285203
|
Nucleutide sequences |
EMBL-CDS:
CAI30569.1,
CAE45897.2,
AGC92970.1,
AAH60887.1,
BAG57436.1,
BAF83045.1,
BAC86479.1
Ensembl_TRS:
ENST00000295571,
ENST00000540764,
ENST00000540955,
ENST00000383701
|
Protein sequencees |
Ensembl_PRO:
ENSP00000373206,
ENSP00000443780,
ENSP00000295571,
ENSP00000444264
RefSeq:
XP_011531901.1,
XP_016861693.1,
XP_005264800.1,
XP_016861696.1,
XP_016861698.1,
NP_001265618.1,
XP_011531904.1,
NP_775925.1,
XP_011531902.1,
XP_011531905.1,
XP_016861697.1,
XP_016861695.1,
XP_016861694.1
|
Others |
UniRef100:
UniRef100_Q5NDL2
UniRef90:
UniRef90_Q5NDL2
UniRef50:
UniRef50_Q5NDL2
UniGene:
Hs.518059
CCDS:
CCDS63684.1,
CCDS2908.1
|
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Refseq |
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