GlyCosmos Portal

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

Displaying entries **3551 - 3575** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0050984	spinocerebellar ataxia type 37	Dab	39866	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110916	hereditary spherocytosis type 1 Aliases: HS1 SPH1 hereditary spherocytosis 1	Spta1	20739	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111286	psoriasis 1 Aliases: PSORS1	HLA-C	3107	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050647	Arts syndrome Aliases: ARTS Lethal ataxia with deafness and optic atrophy MRXS18 MRXSARTS fatal X-linked ataxia with deafness and loss of vision syndromic X-linked mental retardation 18 syndromic X-linked mental retardation Arts type	PITX2 PRPS1 PRPSAP1	5308 5631 5635	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110971	brachydactyly type D Aliases: BDD	HOXD13	3239	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060944	episodic kinesigenic dyskinesia 3	TMEM151A	256472	Homo sapiens (human)	Alliance of Genome Resources
DOID:13381	pernicious anemia Aliases: ANEMIA PERNICIOUS Addison's anaemia Biermer's anaemia Biermer's anemia pernicious anaemia	Cblif	14603	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8432	polycythemia Aliases: Erythrocythemia	Acer Ance	34189 34805	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:10223	dermatomyositis Aliases: Polymyositis with skin involvement dermatopolymyositis	Aars1 Angptl2 Cd36 Cd40 Cd40lg Fas Hgf Ifng Il4 Mbl2 Mmp9 Robo1 Slit2 Thbd Tlr2 Tlr4 Tlr9	12491 14102 15234 15978 16189 17195 17395 19876 20563 21824 21898 21939 21947 234734 24088 26360 81897	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2921	glomerulonephritis	ACE ADM AGT AGTR2 ALOX15 ANXA5 AXL BDKRB1 C1QA C3 C6 CCL1 CCL7 CD163 CD59 CFI CNDP1 COL4A3 CSF1 CX3CL1 EP300 F2 FBN1 FCGR2B FCGR3A FN1 FOS GAS6 GDNF IFNG IL1RN ITGA3 ITGB1 ITGB3 KLKB1 LTBP1 LTC4S MMP3 MPO MS4A1 NGF NPPA PDGFB PDGFD PLA2G7 PRF1 PTAFR SERPINE1 SPP1 TBXAS1 TF TNFRSF1A TNFRSF1B TPO VCAM1 VEGFA	1285 133 1435 1636 183 186 2033 2147 2200 2213 2214 2335 2353 246 2621 2668 308 3426 3458 3557 3675 3688 3690 3818 4052 4056 4314 4353 4803 4878 5054 5155 5551 558 5724 623 6346 6354 6376 6696 6916 7018 712 7132 7133 7173 718 729 7412 7422 7941 80310 84735 931 9332 966	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060775	microvillus inclusion disease Aliases: Davidson disease MVD congenital familial protracted diarrhea with enterocyte brush-border abnormalities congenital microvillus atrophy diarrhea 2 with microvillus atrophy intractable diarrhea of infancy	CDC42	998	Homo sapiens (human)	Alliance of Genome Resources
DOID:9120	amyloidosis Aliases: amyloid disease	Adipoq Apcs Csf1 Got1 Tnf Tnfrsf1a Trem1 Ttr	11450 12977 14718 20219 21926 21937 22139 58217	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2237	hepatitis Aliases: acute and subacute liver necrosis acute hepatitis acute/subac. necrosis of liver animal hepatitis chronic hepatitis chronic persistent hepatitis	gbgt1l2 gbgt1l3 gbgt1l4 gbgt1l5 gbgt1l8 gbgt1l9	100005565 100005704 387303 447881 563897 566487	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:1800	neuroendocrine carcinoma	ENO2	2026	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111056	platelet-type bleeding disorder 3 Aliases: BDPLT3 PT-VWD platelet type-von Willebrand disease pseudo-von Willebrand disease von Willebrand disease platelet-type	GP1BA	2811	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080227	autosomal dominant intellectual developmental disorder 55 Aliases: autosomal dominant intellectual developmental disorder-55 with seizures autosomal dominant mental retardation 55	Nus1	52014	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:543	dystonia Aliases: dystonic disease	Penk Tor1a Tor2a Tor3a	266606 29237 304884 362112	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080685	aortic dissection	ephb1.S	399288	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0080290	familial erythrocytosis 5 Aliases: ECYT5	Epo	24335	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:303	substance-related disorder	Cdh13 Faslg Gsk3b Htr2c Slc18a2	192248 25187 25385 25549 84027	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110297	autosomal recessive limb-girdle muscular dystrophy type 2K Aliases: LGMD2K MDDGC1 limb-girdle muscular dystrophy-intellectual disability syndrome muscular dystrophy limb-girdle type 2K muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1	rt	39297	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2797	idiopathic interstitial pneumonia Aliases: Diffuse idiopathic pulmonary fibrosis Idiopathic fibrosing alveolitis	Icam1	25464	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:769	neuroblastoma	ltk	564470	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0090113	RIDDLE syndrome Aliases: RNF168 deficiency Radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome	RNF168	165918	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111237	congenital muscular dystrophy-dystroglycanopathy type A1 Aliases: MDDGA1 Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1	Pomt1	84430	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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