KEGG   VARIANT: 84892v1
Entry
84892v1                      Variant                               
Name
POMGNT2 deficiency
Gene
POMGNT2  protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) [KO:K18207]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 614828
Network
nt06013  O-Glycan biosynthesis
Disease
H00120  Muscular dystrophy-dystroglycanopathy type A
H01959  Muscular dystrophy-dystroglycanopathy type C
Reference
  Authors
Manzini MC, Tambunan DE, Hill RS, Yu TW, Maynard TM, Heinzen EL, Shianna KV, Stevens CR, Partlow JN, Barry BJ, Rodriguez J, Gupta VA, Al-Qudah AK, Eyaid WM, Friedman JM, Salih MA, Clark R, Moroni I, Mora M, Beggs AH, Gabriel SB, Walsh CA
  Title
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.
  Journal
Am J Hum Genet 91:541-7 (2012)
DOI:10.1016/j.ajhg.2012.07.009
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