GlyCosmos Portal

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

Displaying entries **3826 - 3850** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:305	carcinoma Aliases: epithelial cancer epithelioma malignant Epithelioma	CSF1R CTNNB1 DLG1 EDA EGFR ERBB2 ERBB3 ERBB4 FAT4 FGR FLT1 FLT3 FLT4 HCK HRAS JUP KDR KIT KRAS LATS1 LATS2 LLGL1 LLGL2 NRAS RAB5A RAB5C S1PR2 SALL1 SALL2 SALL4 SCD SCRIB SNAI1 SRC STK4 TNFSF12-TNFSF13 TNFSF12 YAP1	10413 1436 1499 1739 1896 1956 2064 2065 2066 2268 2321 2322 2324 23513 26524 3055 3265 3728 3791 3815 3845 3993 3996 407977 4893 57167 5868 5878 6297 6299 6319 6615 6714 6789 79633 8742 9113 9294	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080006	bone development disease	CSF1R FLNB LRP4 NPR2 TNFRSF11A	1436 2317 4038 4882 8792	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080523	adult-onset leukoencephalopathy with axonal spheroids and pigmented glia Aliases: hereditary diffuse leukoencephalopathy with spheroids	CSF1R	1436	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070343	CSF1R-related brain malformation and osteopetrosis Aliases: osteoporosis and infantile neuroaxonal dystrophy	CSF1R	1436	Homo sapiens (human)	Alliance of Genome Resources
DOID:8692	myeloid leukemia Aliases: Non-Lymphocytic Leukemia leukaemia myelogenous leukemia myelogenous myeloid granulocytic leukaemia myeloid granulocytic leukemia myeloid leukaemia	CSF3 FGFR1 GATA2 IFNG IGFBP3 MN1 MPL NSD3 PDGFRA PECAM1 SNCA UGT1A1	1440 2260 2624 3458 3486 4330 4352 5156 5175 54658 54904 6622	Homo sapiens (human)	Alliance of Genome Resources
DOID:12010	anterior ischemic optic neuropathy Aliases: Ischemic optic neuropathy	CSF3 NOS3	1440 4846	Homo sapiens (human)	Alliance of Genome Resources
DOID:11450	allergic cutaneous vasculitis Aliases: Allergic Cutaneous Angiitis Autoimmune Hypersensitivity angiitis	CSF3	1440	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050590	severe congenital neutropenia	CSF3R ELANE HAX1	10456 1441 1991	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090120	hereditary neutrophilia	CSF3R	1441	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080187	chronic neutrophilic leukemia	CSF3R	1441	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112129	severe congenital neutropenia 7 Aliases: SCN7 autosomal recessive severe congenital neutropenia due to CSF3R deficiency	CSF3R	1441	Homo sapiens (human)	Alliance of Genome Resources
DOID:10595	Charcot-Marie-Tooth disease Aliases: CMT - Charcot-Marie-Tooth disease	CSG2 DPL1 FIG4	851888 852324 855392	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111651	ectodermal dysplasia 15 Aliases: ECTD15 ectodermal dysplasia 15, hypohidrotic/hair type	CST6	1474	Homo sapiens (human)	Alliance of Genome Resources
DOID:3535	Unverricht-Lundborg syndrome Aliases: Unverricht - Lundborg disease Unverricht's disease Unverricht-Lundborg disease	CSTB	1476	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111452	progressive myoclonus epilepsy 1A Aliases: EPM1A	CSTB	1476	Homo sapiens (human)	Alliance of Genome Resources
DOID:3151	skin squamous cell carcinoma Aliases: Epidermoid skin carcinoma	CTCF DDX5 KNSTRN	10664 1655 90417	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080144	childhood acute lymphocytic leukemia Aliases: Childhood Acute Lymphoblastic Leukemia	CTCF	10664	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070051	autosomal dominant intellectual developmental disorder 21 Aliases: MRD21 autosomal dominant mental retardation 21 autosomal dominant non-syndromic intellectual disability 21	CTCF	10664	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090142	cystathioninuria Aliases: cystathionase deficiency cystathione gamma-lyase deficiency syndrome gamma-cystathionase deficiency	CTH	1491	Homo sapiens (human)	Alliance of Genome Resources
DOID:986	alopecia areata Aliases: Circumscribed alopecia	CTLA4 DNMT1 EHMT2 HDAC1 HDAC2 HDAC7 HLA-DQA1 HLA-DQB1 IL1RN IL2 KDM1A KDM4C NOTCH4	10919 1493 1786 23028 23081 3065 3066 3117 3119 3557 3558 4855 51564	Homo sapiens (human)	Alliance of Genome Resources
DOID:7188	autoimmune thyroiditis Aliases: Chronic Lymphocytic Thyroiditis Hashimoto thyroiditis Hashimoto's Disease Hashimoto's syndrome Hashimoto's thyroiditis Lymphocytic Thyroiditis	CTLA4 HLA-DQA1 HLA-DQB1 HLA-DRA HLA-DRB1 IFNG IL4 LRP2 MBL2 TG TLR3	1493 3117 3119 3122 3123 3458 3565 4036 4153 7038 7098	Homo sapiens (human)	Alliance of Genome Resources
DOID:9383	iridocyclitis Aliases: primary iridocyclitis	CTLA4 HLA-DQB1 ICAM1 IL1A	1493 3119 3383 3552	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060025	immunoglobulin alpha deficiency Aliases: IgA deficiency gamma-A-globulin deficiency	CTLA4 HLA-DQB1 ICOS	1493 29851 3119	Homo sapiens (human)	Alliance of Genome Resources
DOID:11168	anogenital venereal wart Aliases: Anogenital Human papilloma Virus Infectious Disease Anogenital warts Genital warts genital wart virus infectious disease venereal wart	CTLA4 IL10 IL12B IL21 IL2 IL4 IL6 KLRK1 MYD88 NCR1 PDCD1 PTPN11 PTPN6 SERPINF1 TGFB1 TLR2 TLR3 TLR4 TLR7 TLR8 TLR9 TNF TNFRSF18	1493 22914 3558 3565 3569 3586 3593 4615 51284 51311 5133 5176 54106 5777 5781 59067 7040 7097 7098 7099 7124 8784 9437	Homo sapiens (human)	Alliance of Genome Resources
DOID:7442	monoclonal gammopathy of uncertain significance Aliases: MGUS Monoclonal gammopathy of undetermined significance	CTLA4 MYD88 NEFH	1493 4615 4744	Homo sapiens (human)	Alliance of Genome Resources

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