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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024

Displaying entries **71601 - 71625** of **71927** in total

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence Code Names ▼	References
DOID:0060540	Hermansky-Pudlak syndrome 2	MGI:1333879	Mus musculus (house mouse)	11774	Ap3b1	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:9434937
DOID:0111809	syndromic microphthalmia 2	MGI:1918708	Mus musculus (house mouse)	71458	Bcor	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:32692983
DOID:0080070	mucolipidosis II alpha/beta	MGI:3643902	Mus musculus (house mouse)	432486	Gnptab	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:17962477 PMID:24127423 PMID:25107912 PMID:26857995
DOID:0060741	methylmalonic acidemia due to transcobalamin receptor defect	MGI:1860083	Mus musculus (house mouse)	54219	Cd320	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:23430977
DOID:6000	congestive heart failure	MGI:104798	Mus musculus (house mouse)	21926	Tnf	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:9577949
DOID:0080051	acromesomelic dysplasia, Hunter-Thompson type	MGI:95688	Mus musculus (house mouse)	14563	Gdf5	author statement supported by traceable reference evidence used in automatic assertion	MGI:5509308 MGI:6194238
DOID:0110593	autosomal dominant nonsyndromic deafness 9	MGI:1278313	Mus musculus (house mouse)	12810	Coch	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:18697796 PMID:21073934
DOID:0110087	asphyxiating thoracic dystrophy 3	MGI:107736	Mus musculus (house mouse)	110350	Dync2h1	author statement supported by traceable reference evidence used in automatic assertion	MGI:5284969 MGI:6194238
DOID:0110480	autosomal recessive nonsyndromic deafness 22	MGI:2149209	Mus musculus (house mouse)	246190	Otoa	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:23129639
DOID:10584	retinitis pigmentosa	MGI:2679260	Mus musculus (house mouse)	241324	Crb2	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:23001562 PMID:24493795
DOID:3265	chronic granulomatous disease	MGI:88574	Mus musculus (house mouse)	13058	Cybb	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:19234224 PMID:7719350
DOID:9744	type 1 diabetes mellitus	MGI:107418	Mus musculus (house mouse)	19276	Ptprn2	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:12535631
DOID:8398	osteoarthritis	MGI:1328350	Mus musculus (house mouse)	17182	Matn3	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:16877353
DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency	MGI:97239	Mus musculus (house mouse)	17850	Mmut	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:14555645 PMID:17937813 PMID:23898205 PMID:27519416 PMID:34901307
DOID:9245	Alagille syndrome	MGI:1095416	Mus musculus (house mouse)	16449	Jag1	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:10196361 PMID:11259677 PMID:21062863 PMID:22156581 PMID:23095891 PMID:29162437
DOID:0110678	congenital myasthenic syndrome 4A	MGI:87894	Mus musculus (house mouse)	11448	Chrne	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:9151734
DOID:0110224	Brugada syndrome 7	MGI:1918882	Mus musculus (house mouse)	235281	Scn3b	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:19351516
DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions	MGI:95832	Mus musculus (house mouse)	14824	Grn	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:25155018 PMID:29382817 PMID:29511098
DOID:1270	hereditary hemorrhagic telangiectasia	MGI:95392	Mus musculus (house mouse)	13805	Eng	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:10348742 PMID:10562296 PMID:10625534 PMID:24520391 PMID:25082229
DOID:0080101	Compton-North congenital myopathy	MGI:105980	Mus musculus (house mouse)	12805	Cntn1	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:25917818
DOID:0050638	transthyretin amyloidosis	MGI:98865	Mus musculus (house mouse)	22139	Ttr	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:11310831 PMID:29360446
DOID:5419	schizophrenia	MGI:2136886	Mus musculus (house mouse)	65079	Rtn4r	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:18043741 PMID:21645550
DOID:1838	Menkes disease	MGI:96817	Mus musculus (house mouse)	16948	Lox	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:12473682
DOID:0060062	familial juvenile hyperuricemic nephropathy	MGI:102674	Mus musculus (house mouse)	22242	Umod	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:15522986 PMID:20472742
DOID:0050588	muscular dystrophy-dystroglycanopathy type B1	MGI:2447586	Mus musculus (house mouse)	243853	Fkrp	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:20675713 PMID:26306834

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