Gene table: search width pubmed_id = 23856421


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital disorder of glycosylation, type Ie - (AR)
2.41
23856421
DPM1 (20q13.13)
Dolichyl-phosphate mannosyltransferase 1, catalytic subunit
* Congenital muscular dystrophy with hypoglycosylation of dystroglycan - CDG1E