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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 **11401 - 11425** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0080055	achondrogenesis type IB Aliases: achondrogenesis Fraccaro type	Slc26a2	13521	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050581	brachydactyly	Slc26a2	13521	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14687	diastrophic dysplasia	Slc26a2	13521	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060296	congenital secretory chloride diarrhea 1 Aliases: congenital chloride diarrhea finnish type congenital chloride diarrhoea finnish type congenital chloridorrhea congenital secretory chloride diarrhoea 1	Slc26a3	114629	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060296	congenital secretory chloride diarrhea 1 Aliases: congenital chloride diarrhea finnish type congenital chloride diarrhoea finnish type congenital chloridorrhea congenital secretory chloride diarrhoea 1	Slc26a3	13487	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110513	autosomal recessive nonsyndromic deafness 61 Aliases: DFNB61 autosomal recessive deafness 61	Slc26a5	80979	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110513	autosomal recessive nonsyndromic deafness 61 Aliases: DFNB61 autosomal recessive deafness 61	Slc26a5	83819	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070168	spermatogenic failure 3 Aliases: SPGF3	Slc26a8	224661	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6652	diffuse idiopathic skeletal hyperostosis Aliases: Ankylosing vertebral hyperostosis DISH Disseminated idiopathic skeletal hyperostosis	Slc29a1	63959	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:6652	diffuse idiopathic skeletal hyperostosis Aliases: Ankylosing vertebral hyperostosis DISH Disseminated idiopathic skeletal hyperostosis	Slc29a1	63997	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111278	histiocytosis-lymphadenopathy plus syndrome Aliases: Faisalabad histiocytosis H syndrome HJCD PHID Rosai–Dorfman disease SHML cutaneous hyperpigmentation with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss familial Rosai-Dorfman disease histiocytosis and lymphadenopathy with or without cutaneous, cardiac, and/or endocrine features, joint contractures and/or deafness histiocytosis with joint contractures and sensorineural deafness pigmented hypertrichosis with insulin-dependent diabetes mellitus sinus histiocytosis and massive lymphadenopathy	Slc29a3	353307	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111278	histiocytosis-lymphadenopathy plus syndrome Aliases: Faisalabad histiocytosis H syndrome HJCD PHID Rosai–Dorfman disease SHML cutaneous hyperpigmentation with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss familial Rosai-Dorfman disease histiocytosis and lymphadenopathy with or without cutaneous, cardiac, and/or endocrine features, joint contractures and/or deafness histiocytosis with joint contractures and sensorineural deafness pigmented hypertrichosis with insulin-dependent diabetes mellitus sinus histiocytosis and massive lymphadenopathy	Slc29a3	71279	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090045	childhood onset GLUT1 deficiency syndrome 2	Slc2a1	20525	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111313	idiopathic generalized epilepsy 12 Aliases: EIG12	Slc2a1	20525	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090044	dystonia 9	Slc2a1	20525	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060326	myelomeningocele	Slc2a1	20525	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111313	idiopathic generalized epilepsy 12 Aliases: EIG12	Slc2a1	24778	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0090045	childhood onset GLUT1 deficiency syndrome 2	Slc2a1	24778	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0090044	dystonia 9	Slc2a1	24778	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060326	myelomeningocele	Slc2a1	24778	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3138	acanthosis nigricans Aliases: keratosis nigricans	Slc2a3 Tbc1d4	20527 210789	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3138	acanthosis nigricans Aliases: keratosis nigricans	Slc2a3	25551	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110794	hereditary spastic paraplegia 42 Aliases: SPG42 autosomal dominant spastic paraplegia 42 autosomal dominant spastic paraplegia type 42	Slc33a1	11416	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110794	hereditary spastic paraplegia 42 Aliases: SPG42 autosomal dominant spastic paraplegia 42 autosomal dominant spastic paraplegia type 42	Slc33a1	64018	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050947	hereditary hypophosphatemic rickets with hypercalciuria	Slc34a1 Slc34a3	142681 20505	Mus musculus (house mouse)	Alliance of Genome Resources

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