GlyCosmos Portal

Displaying entries **401 - 425** of **919** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
39436	Phosphomannomutase type 2	Pmm2	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congenital disorder of glycosylation
39435	Transferrin 2	Tsf2
39409	Corazonin receptor	CrzR
39404	Inositol polyphosphate 5-phosphatase E	INPP5E	Joubert syndrome 1 Joubert syndrome obesity
39393	Esterase P	Est-P
39392	Esterase 6	Est-6
39387	Neurexin IV	Nrx-IV
39383	Autophagy-related 12	Atg12
39324	Gustatory receptor 68a	Gr68a
39321	crimpled	crim
39297	rotated abdomen	rt	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
39265	procollagen lysyl hydroxylase	Plod	Bruck syndrome Ehlers-Danlos syndrome kyphoscoliotic type 1 Ehlers-Danlos syndrome hepatocellular carcinoma hypothyroidism lung adenocarcinoma
39262	Glucuronyltransferase P	GlcAT-P
39259	wntless	wls
39218	uncharacterized protein	CG6418
39215	Ninjurin A	NijA
39204	CTD nuclear envelope phosphatase 1 regulatory subunit 2	Cnep1r2
39180	defective proboscis extension response 10	dpr10
39118	Laminin B2	LanB2
39106	pathetic	path
39103	Jumonji, AT rich interactive domain 2	Jarid2
39098	uncharacterized protein	CG3434
39064	Peptidoglycan recognition protein LF	PGRP-LF
39063	Peptidoglycan recognition protein LC	PGRP-LC	lower respiratory tract disease
39062	Peptidoglycan recognition protein LA	PGRP-LA