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285203 EOGT

285203

EOGT

EGF domain specific O-linked N-acetylglucosamine transferase

protein-coding

Homo sapiens

基因描述

Type Description
Definition EGF domain specific O-linked N-acetylglucosamine transferase

研究结论

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

名称对应

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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