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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 **11626 - 11650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:9997	peripartum cardiomyopathy Aliases: antepartum peripartum cardiomyopathy postpartum peripartum cardiomyopathy	Stat3	20848	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080836	growth hormone insensitivity syndrome with immune dysregulation 1	Stat5a Stat5b	20850 20851	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080909	castration-resistant prostate carcinoma	Stat5a	20850	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080837	growth hormone insensitivity syndrome with immune dysregulation 2	Stat5b	20851	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080089	tubular aggregate myopathy 1	Stim	32556	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060354	Stormorken syndrome Aliases: thrombocytopathy, asplenia and miosis	Stim	32556	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111970	immunodeficiency 10 Aliases: CID due to STIM1 deficiency IMD10 STIM1 deficiency combined immunodeficiency due to STIM1 deficiency immune dysfunction with T-cell inactivation due to calcium entry defect 2	Stim	32556	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:12387	nephrogenic diabetes insipidus	Stim	32556	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060354	Stormorken syndrome Aliases: thrombocytopathy, asplenia and miosis	Stim1	20866	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080089	tubular aggregate myopathy 1	Stim1	20866	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111970	immunodeficiency 10 Aliases: CID due to STIM1 deficiency IMD10 STIM1 deficiency combined immunodeficiency due to STIM1 deficiency immune dysfunction with T-cell inactivation due to calcium entry defect 2	Stim1	20866	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080089	tubular aggregate myopathy 1	Stim1	361618	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060354	Stormorken syndrome Aliases: thrombocytopathy, asplenia and miosis	Stim1	361618	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111970	immunodeficiency 10 Aliases: CID due to STIM1 deficiency IMD10 STIM1 deficiency combined immunodeficiency due to STIM1 deficiency immune dysfunction with T-cell inactivation due to calcium entry defect 2	Stim1	361618	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111457	STING-associated vasculopathy with onset in infancy Aliases: SAVI	Sting	36016	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111807	syndromic microphthalmia 9 Aliases: Matthew-Wood syndrome anophthalmia-pulmonary hypoplasia syndrome anophthalmia/microphthalmia and pulmonary hypoplasia clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations pulmonary agenesis microphthalmi and diaphragmatic defect spear syndrome	Stra6	20897	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111807	syndromic microphthalmia 9 Aliases: Matthew-Wood syndrome anophthalmia-pulmonary hypoplasia syndrome anophthalmia/microphthalmia and pulmonary hypoplasia clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations pulmonary agenesis microphthalmi and diaphragmatic defect spear syndrome	Stra6	363071	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110471	autosomal recessive nonsyndromic deafness 16 Aliases: DFNB16 autosomal recessive deafness 16	Strc	140476	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1700	X-linked ichthyosis Aliases: X-linked ichthyosis with steryl-sulphatase deficiency X-linked placental steryl-sulphatase deficiency X-linked recessive ichthyosis	Sts	24800	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080572	congenital disorder of glycosylation Iw Aliases: congenital disorder of glycosylation 1w	Stt3A Stt3B	33082 43005	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080573	congenital disorder of glycosylation Ix Aliases: congenital disorder of glycosylation 1x	Stt3B	43005	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080572	congenital disorder of glycosylation Iw Aliases: congenital disorder of glycosylation 1w	Stt3a Stt3b	16430 68292	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080572	congenital disorder of glycosylation Iw Aliases: congenital disorder of glycosylation 1w	Stt3a Stt3b	363160 500972	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080573	congenital disorder of glycosylation Ix Aliases: congenital disorder of glycosylation 1x	Stt3b	363160	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080573	congenital disorder of glycosylation Ix Aliases: congenital disorder of glycosylation 1x	Stt3b	68292	Mus musculus (house mouse)	Alliance of Genome Resources

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