KEGG   VARIANT: 10195v1
Entry
10195v1                      Variant                               
Name
ALG3 deficiency
Gene
ALG3  ALG3 alpha-1,3- mannosyltransferase [KO:K03845]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 608750
Network
nt06015  N-Glycan biosynthesis
Disease
H00118  Congenital disorders of glycosylation type I
Reference
  Authors
Denecke J, Kranz C, Kemming D, Koch HG, Marquardt T
  Title
An activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id).
  Journal
Hum Mutat 23:477-86 (2004)
DOI:10.1002/humu.20026
LinkDB

DBGET integrated database retrieval system