GlyCosmos Portal

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

Displaying entries **3626 - 3650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0050921	pharynx squamous cell carcinoma	CLPTM1L	81037	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110828	Usher syndrome type 3 Aliases: USH3	CLRN1	7401	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110841	Usher syndrome type 3A Aliases: USH3A Usher syndrome type IIIA	CLRN1	7401	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110373	retinitis pigmentosa 61 Aliases: RP61	CLRN1	7401	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080226	autosomal dominant intellectual developmental disorder 56 Aliases: autosomal dominant intellectual developmental disorder-56 autosomal dominant mental retardation 56	CLTC	1213	Homo sapiens (human)	Alliance of Genome Resources
DOID:8691	mycosis fungoides Aliases: mycosis fungoides lymphoma	CLU HIF1A HLA-DQB1 SOD2	1191 3091 3119 6648	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050426	Stevens-Johnson syndrome	CLU HLA-A HLA-B HLA-DQB1 TNF	1191 3105 3106 3119 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:11656	cicatricial pemphigoid Aliases: Cicatricial pemphigoid with ocular involvement Ocular pemphigoid benign mucous membrane pemphigoid benign mucous membrane pemphigoid with ocular involvement ocular pemphigus	CLU HLA-DQB1 HLA-DRB1 IL1RN TNF	1191 3119 3123 3557 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:4251	conjunctival disease	CLU IL6 TNFAIP6	1191 3569 7130	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060449	gelatinous drop-like corneal dystrophy Aliases: GDCD corneal amyloidosis primary familial amyloidosis of the cornea subepithelial amyloidosis of the cornea	CLU TACSTD2	1191 4070	Homo sapiens (human)	Alliance of Genome Resources
DOID:4930	nasal cavity adenocarcinoma Aliases: adenocarcinoma of the nasal cavity	CLU	1191	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060307	autosomal dominant intellectual developmental disorder Aliases: autosomal dominant mental retardation autosomal dominant non-syndromic mental retardation	CMR2 GIS1 SSN2	851670 852053 854260	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9970	obesity	CNE1 DPL1 ECM14 EMI2 GCY1 GLK1 HFA1 HXK1 HXK2 IZH1 KEX2 NPP1 NPP2 PEP4 POX1 PUF3 RHO1 SEC16 SLA1 SRB8 SSN2 TDH1 TDH2 TDH3 TRM732 VVS1 YOL075C YPR1 ZWF1	850317 850391 850442 850614 850647 851241 851888 851974 852053 852102 852128 852276 852543 852639 852667 853106 853395 853465 854080 854287 855247 855301 855480 855483 855949 856020 856294 856533 856699	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110377	retinitis pigmentosa 49 Aliases: RP49	CNGA1	1259	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110007	achromatopsia 2 Aliases: ACHM2 RMCH2 rod monochromacy 2 rod monochromatism 2	CNGA3	1261	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110402	retinitis pigmentosa 45 Aliases: RP45	CNGB1	1258	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080242	syndromic X-linked mental retardation Hough type	CNKSR2	22866	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060884	renal hypomagnesemia 6 Aliases: HOMG6	CNNM2	54805	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111404	Jalili syndrome Aliases: Cone rod dystrophy-amelogenesis imperfecta syndrome cone-rod dystrophy and amelogenesis imperfecta	CNNM4	26504	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081398	holoprosencephaly 12 Aliases: holoprosencephaly-12 with or without pancreatic agenesis	CNOT1	23019	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081397	Vissers-Bodmer syndrome	CNOT1	23019	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080432	developmental and epileptic encephalopathy 60 Aliases: DEE60 early infantile epileptic encephalopathy 60	CNPY3	10695	Homo sapiens (human)	Alliance of Genome Resources
DOID:750	peptic ulcer disease Aliases: acute peptic ulcer with hemorrhage acute peptic ulcer with hemorrhage and perforation acute peptic ulcer without hemorrhage and without perforation	CNR1 CYP2C19 HLA-DRB1	1268 1557 3123	Homo sapiens (human)	Alliance of Genome Resources
DOID:2234	focal epilepsy Aliases: localisation-related epilepsy partial epilepsy	CNR1 DEPDC5 MMP9	1268 4318 9681	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080101	Compton-North congenital myopathy Aliases: congenital myopathy 12	CNTN1	1272	Homo sapiens (human)	Alliance of Genome Resources

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