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440138 ALG11

440138

ALG11

ALG11 alpha-1,2-mannosyltransferase

protein-coding

Homo sapiens

基因描述

Type Description
Definition ALG11 alpha-1,2-mannosyltransferase

研究结论

Date Results Publications
2015-04-04 13:00:00 Hence, we concluded that there is different transcriptional control mechanism between mALG11 and hALG11 25036826
2012-06-09 11:47:00 After identifying the congenital disorders of glycosylation-Ip index patient, study describe three more cases suffering from an ALG11 deficiency. 22213132
2010-09-20 12:29:00 Deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation. 20080937

名称对应

Type IDs
Synonymous CDG1P, GT8
Gene
UniProtKB-ID: ALG11_HUMAN
UniprotKB: Q2TAA5
UniParc: UPI000044C60E
EMBL: BC111022, BC073862, AK296747, BC142998, AL139082, BC010857
Ensembl: ENSG00000253710
KO: hsa:440138
Nucleutide sequences
EMBL-CDS: AAI42999.1, AAI11023.1, AAH73862.1, AAH10857.3, BAG59331.1
Ensembl_TRS: ENST00000521508
Protein sequencees
Ensembl_PRO: ENSP00000430236
RefSeq: NP_001004127.2
Others
UniRef100: UniRef100_Q2TAA5
UniRef90: UniRef90_Q2TAA5
UniRef50: UniRef50_Q2TAA5
UniGene: Hs.512963, Hs.732220
CCDS: CCDS31977.1

全选

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研究热度

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