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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 **12476 - 12500** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:12849	autistic disorder Aliases: Kanner's syndrome autism autistic disorder of childhood onset childhood autism infantile autism	ANK2 C4B CCL2 CNTNAP2 DAB1 EIF4E EN2 FOXP2 GABRA2 GABRA4 GABRA5 GABRB1 GABRB2 GABRR2 GLO1 GRM8 GRN HLA-DRB1 HRAS HSPD1 IL6 KCNQ3 KDM4C KMT2E LAMB1 MECP2 MET MTR NF1 NLGN1 NLGN3 NLGN4X NTRK2 PECAM1 PIK3CG PTCHD1 RELN RPP25 SETDB1 SHANK2 SLC25A12 SLC6A4 SLC9A9 TNF VLDLR	139411 1600 1977 2020 22871 22941 23081 2555 2557 2558 2560 2561 2570 26047 2739 285195 287 2896 2918 3123 3265 3329 3569 3786 3912 4204 4233 4548 4763 4915 5175 5294 54413 54913 55904 5649 57502 6347 6532 7124 721 7436 8604 93986 9869	Homo sapiens (human)	Alliance of Genome Resources
DOID:2340	craniosynostosis Aliases: Premature closure of cranial sutures	Bbs9 Erf Fgfr2 Nell1 Nog Tcf12	13875 14183 18121 21406 319845 338352	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050598	extrapulmonary tuberculosis	Cd209a Cd209b Cd209c Cd209d Ereg	13874 170776 170779 170786 69165	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:869	cholesteatoma	Ereg Hgf Il1a Mmp2 Mmp9 Tlr2 Tlr4 Vegfa	13874 15234 16175 17390 17395 21898 22339 24088	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1933	Rubinstein-Taybi syndrome Aliases: Broad Thumb-Hallux syndrome Rubinstein syndrome proximal chromosome 16p13.3 deletion syndrome	CREBBP EP300	1387 2033	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060210	amyotrophic lateral sclerosis type 19 Aliases: ALS19 amyotrophic lateral sclerosis 19	Erbb4	13869	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4306	radiculopathy Aliases: pinched nerve	Erbb4 Spp1 Tnf	13869 20750 21926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060560	lethal congenital contracture syndrome 2 Aliases: LCCS2 multiple contracture syndrome, Israeli-Bedouin type	Erbb3	13867	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080679	neuronal intestinal dysplasia type A	Erbb3	13867	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3443	mammary Paget's disease Aliases: Paget cell neoplasm Paget's disease Paget's disease of the breast mammary Paget disease	Erbb2	13866	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13133	HELLP syndrome	Adamts13 Cd40lg Erbb2 Fas Fasl	13866 14102 14103 21947 279028	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10376	amblyopia Aliases: lazy eye	Erbb2 Erbb3 Erbb4 Ppargc1a	13866 13867 13869 19017	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110463	autosomal recessive nonsyndromic deafness 102 Aliases: DFNB102 autosomal recessive deafness 102	Eps8	13860	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11049	meconium aspiration syndrome Aliases: Neonatal aspiration of meconium meconium aspiration	AGT AGTR2 ATF2	1386 183 186	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060652	familial erythrocytosis 1 Aliases: ECYT1 autosomal dominant benign erythrocytosis primary familial and congenital polycythemia	Epor	13857	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13413	hepatic encephalopathy Aliases: Portal-systemic encephalopathy	Abcb1b Ccl2 Epor G6pd2 G6pdx Gabra1 Gabrb1 Gabrg2 Gc Glud1 Gria1 Insr Ptgs1	13857 14380 14381 14394 14400 14406 14473 14661 14799 16337 18669 19224 20296	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080290	familial erythrocytosis 5 Aliases: ECYT5	Epo	13856	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13268	porphyria Aliases: Hematoporphyria Porphyrinopathy disorder of porphyrin and hem metabolism disorder of porphyrin metabolism	Epo Gbe1	13856 74185	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9973	substance dependence	CREB1 FOSB	1385 2354	Homo sapiens (human)	Alliance of Genome Resources
DOID:11206	opioid abuse	CREB1 DRD4 FOSB GRIN1 GRIN2A GRIN2B NCAM1 NR3C1 OPRD1 OPRK1 OPRM1	1385 1815 2354 2902 2903 2904 2908 4684 4985 4986 4988	Homo sapiens (human)	Alliance of Genome Resources
DOID:11870	Pick's disease Aliases: Dementia in Pick's disease LOBAR ATROPHY OF BRAIN PICK DISEASE OF BRAIN Pick disease	ATF2 CREB1 FOS MAP2K6 MAPT SNCA SNCB TARDBP	1385 1386 23435 2353 4137 5608 6620 6622	Homo sapiens (human)	Alliance of Genome Resources
DOID:10320	asbestosis	Ephx1 Tnc	13849 21923	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:705	Leber hereditary optic neuropathy Aliases: Leber's hereditary optic neuropathy Leber's optic atrophy	Ephx1 ND5 Sod2 Trp53	13849 17721 20656 22059	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5022	aflatoxins-related hepatocellular carcinoma	Ephx1 Ggt1	13849 14598	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080001	bone disease	Ephx1 Fgfr1 Fgfr2 Fgfr4 Npr3 Pon1	13849 14182 14183 14186 18162 18979	Mus musculus (house mouse)	Alliance of Genome Resources

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