GlyCosmos Portal

Homo sapiens (human)

Summary

Gene Symbol	Gene Symbol Aliases	Gene ID	Disease Name ▲
B4GALT7	XGALT-1 beta4Gal-T7 galactosyltransferase I	11285	B4GALT7-CDG
MANBA	beta-mannosidase A	4126	Beta-mannosidosis
COG1	KIAA1381	9382	COG1-CDG
COG4	COD1 DKFZP586E1519	25839	COG4-CDG
COG5	GTC90	10466	COG5-CDG
COG6	COD2 KIAA1134	57511	COG6-CDG
COG7		91949	COG7-CDG
COG8	DOR1 FLJ22315	84342	COG8-CDG
FKTN	LGMD2M	2218	Cardiomyopathy, dilated, 1X Fukuyama congenital muscular dystrophy Muscular dystrophy, limb-girdle, type 2M
PSAP	saposin-A saposin-B saposin-C saposin-D variant Gaucher disease and variant metachromatic leukodystrophy	5660	Combined saposin deficiency Gaucher disease, atypical, due to saposin C deficiency Metachromatic leukodystrophy, due to saposin B deficiency