Gene table: search width pubmed_id = 23109149


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital disorder of glycosylation, type 1u - (AR)
2.43
23109149
DPM2 (9q34.13)
Dolichyl-phosphate mannosyltransferase polypeptide 2, regulatory subunit
* Muscle dystrophy with congenital disorder of glycosylation
* Congenital muscular dystrophy and abnormal glycosylation of dystroglycan with se