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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **5701 - 5725** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:0110263	cataract 19 multiple types Aliases: CTRCT19	Lim2	114903	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110263	cataract 19 multiple types Aliases: CTRCT19	Lim2	233187	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110263	cataract 19 multiple types Aliases: CTRCT19	LIM2	3982	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110264	cataract 33 Aliases: CTRCT33	BFSP1	631	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110265	cataract 31 multiple types Aliases: CTRCT31	CHMP4B	128866	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110266	cataract 9 multiple types Aliases: CTRCT9 cataract 9 multiple types with or without microcornea	CRYAA	1409	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110266	cataract 9 multiple types Aliases: CTRCT9 cataract 9 multiple types with or without microcornea	Cryaa	24273	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110266	cataract 9 multiple types Aliases: CTRCT9 cataract 9 multiple types with or without microcornea	Cryaa	12954	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110267	cataract 44 Aliases: CTRCT44 total early-onset cataract	LSS	4047	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110272	cataract 40 Aliases: CTRCT40 cataract 40 X-linked cataract 40 with or without microcornea	NHS	4810	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110273	autosomal dominant limb-girdle muscular dystrophy	CAPN3	825	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	Hmgcr Jag2 Lama2 Poglut1 Pomt2 Popdc3	15357 16450 16773 217734 224143 78977	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	lam-3	172952	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	HMGCR JAG2 LAMA2 POGLUT1 POMT2 POPDC3	29954 3156 3714 3908 56983 64208	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	poglut1 pomt2	563878 641495	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	pomt2	100490100	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	Hmgcr Poglut1 Pomt2	25675 288091 688673	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	HMG1 HMG2 PMT2 PMT3 PMT6	851171 851210 853113 854499 854900	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	hmgcr.L pomt2.L	108698684 397750	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	Hmgcr Ser rumi tn tw	31024 326122 37190 42803 43275	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A Aliases: LGMD2A Leyden-Moebius muscular dystrophy limb-girdle muscular dystrophy due to calpain deficiency muscular dystrophy, limb-girdle, type 2A pelvofemoral muscular dystrophy primary calpainopathy	CAPN3	825	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B Aliases: LGMD2B LGMD3 limb-girdle muscular dystrophy due to dysferlin deficiency limb-girdle muscular dystrophy type 3	Dysf	26903	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C Aliases: DMDA1 LGMD2C Maghrebian myopathy SCARMD autosomal recessive Duchenne-like muscular dystrophy type 1 deficiency of sarcoglycan gamma gamma-sarcoglycanopathy limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency muscular dystrophy, limb-girdle, type 2C severe childhood autosomal recessive muscular dystrophy North African type	Sgcg	24053	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C Aliases: DMDA1 LGMD2C Maghrebian myopathy SCARMD autosomal recessive Duchenne-like muscular dystrophy type 1 deficiency of sarcoglycan gamma gamma-sarcoglycanopathy limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency muscular dystrophy, limb-girdle, type 2C severe childhood autosomal recessive muscular dystrophy North African type	SGCG	6445	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D Aliases: Alpha-sarcoglycanopathy DMDA2 Duchenne-like autosomal recessive muscular dystrophy type 2 LGMD2D muscular dystrophy, limb-girdle, type 2D primary adhalinopathy	DAG1 SGCA	1605 6442	Homo sapiens (human)	Alliance of Genome Resources

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