GlyCosmos Portal

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

Displaying entries **15626 - 15650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0080899	lung pleomorphic carcinoma	SLC3A2 SLC7A5	6520 8140	Homo sapiens (human)	Alliance of Genome Resources
DOID:529	blepharospasm	dop-1	180714	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080092	myofibrillar myopathy 1 Aliases: autosomal recessive limb-girdle muscular dystrophy type 2R desminopathy	DES LDB3	11155 1674	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070042	Coffin-Siris syndrome 1 Aliases: CSS1 MRD12 autosomal dominant mental retardation 12 fifth digit syndrome	Arid1a	93760	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081423	familial focal epilepsy with variable foci 3	DEPDC5 NPRL3	8131 9681	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080086	nonsyndromic congenital nail disorder 8 Aliases: isolated toenail dystrophy	Col7a1	12836	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050579	glycogen storage disease XV Aliases: Glycogen storage disease 15 Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency glycogen storage disease type XV	Gyg1	81675	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3068	glioblastoma Aliases: GBM adult glioblastoma multiforme glioblastoma multiforme grade IV adult Astrocytic tumor primary glioblastoma multiforme spongioblastoma multiforme	kdr	554230	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0050630	Aland Island eye disease Aliases: FORSIUS-ERIKSSON TYPE OCULAR ALBINISM Forsius-Eriksson syndrome	cacna1f.L	100462913	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0111232	congenital muscular dystrophy-dystroglycanopathy type A9 Aliases: MDDGA9 Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9	DAG1	1605	Homo sapiens (human)	Alliance of Genome Resources
DOID:540	strabismus	bmp4.S	399322	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:9505	cannabis abuse Aliases: marijuana abuse	BCHE COMT DRD4 NGF NRG1	1312 1815 3084 4803 590	Homo sapiens (human)	Alliance of Genome Resources
DOID:10247	pleurisy	ALOX5 ANXA1 BDKRB1 BDKRB2 CCL11 CSF3 ELANE ESR1 ICAM1 IL15 IL17A IL1RN NOS2 PLA2G6 PTAFR PTGS2 SERPINE1 TNF	1440 1991 2099 240 301 3383 3557 3600 3605 4843 5054 5724 5743 623 624 6356 7124 8398	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110589	autosomal dominant nonsyndromic deafness 68 Aliases: DFNA68 autosomal dominant deafness 68	homer	33944	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4074	pancreatic adenocarcinoma Aliases: pancreas adenocarcinoma	ADGRB1 AKT3 CXCR4 E2F1 HRG JAK1 MAP2K1 MAPK9 NFKB1 PLAT RAC1 RAF1 VEGFC	10000 1869 3273 3716 4790 5327 5601 5604 575 5879 5894 7424 7852	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050570	congenital disorder of glycosylation type I	Alg12 Alg1 Alg9 Dolk Dpm1 Dpm3 Pmm2 gny wol xit	31623 34134 34409 35240 36856 3885575 39436 41191 42146 43031	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110425	dilated cardiomyopathy 1A Aliases: CDCD1 dilated cardiomyopathy with conduction defect 1 familial dilated cardiomyopathy with conduction defect due to LMNA mutation	DOT1L LMNA LMNB1 LMNB2	4000 4001 84444 84823	Homo sapiens (human)	Alliance of Genome Resources
DOID:1927	sphingolipidosis Aliases: sphingolipidoses	Asah1	84431	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:543	dystonia Aliases: dystonic disease	Atp2b4 Bche Gnal Penk Tor1a Tor1b Tor2a Tor3a	12038 14680 18619 30931 30933 30934 30935 381290	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050476	Barth syndrome Aliases: 3-methylglutaconicaciduria type 2 3-methylglutaconicaciduria type II MGA Type 2 MGA type II	Mest	58827	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110182	Charcot-Marie-Tooth disease axonal type 2C Aliases: CMT2C Charcot-Marie-Tooth neuropathy type 2C HMSN2C autosomal cominant axonal Charcot-Marie-Tooth disease type 2C autosomal dominant Charcot-Marie-Tooth disease type 2C hereditary motor and sensory neuropathy type IIc	Trpv4	63873	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050590	severe congenital neutropenia	CSF3R ELANE HAX1	10456 1441 1991	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080540	galactosialidosis	Ctsa	19025	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2394	ovarian cancer Aliases: malignant Ovarian tumor malignant tumour of ovary ovarian neoplasm ovary neoplasm primary ovarian cancer tumor of the Ovary	ATG26 CTS2 OGG1 STE6 TRE1 TRE2 VPS70	850886 851977 853590 853671 854430 854942 855927	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:8778	Crohn's disease Aliases: Crohn disease Crohn's disease of colon Crohn's disease of large bowel Granulomatous Colitis Pediatric Crohn's disease	Abcb1a Abcb1b Adipoq Alpi Alppl2 Bpi Cd40 Chrna7 Col6a3 Esr2 F13a1 F2 Fcgr2b Fcgr3 Fcgr4 Fga Fgf7 Gc Gpx1 H2-Ab1 Hfe Icam1 Ifng Il10 Il21r Il23r Kdr Mbl2 Mki67 Pgf Plaur Pon1 Pon3 Prf1 Ptgs2 Sell Slc11a1 Slc22a21 Slc22a5 Stat3 Thbd Tnf Tnfrsf1a Tnfrsf1b Ugt1a1 Vegfa Vipr1	11441 11450 11650 12835 13983 14061 14130 14131 14161 14178 14473 14775 14961 15216 15894 15978 16153 16542 17195 17345 18173 18646 18654 18669 18671 18793 18979 19225 20343 20520 20848 209590 21824 21926 21937 21938 21939 22339 22354 246256 269823 329547 394436 56517 60504 74145 76768	Mus musculus (house mouse)	Alliance of Genome Resources

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