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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

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	FlyGlycoDB	Evidence Code Names	References ▼
DOID:0111041	glycogen storage disease IXb	MGI:97578	Mus musculus (house mouse)	102093	Phkb		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:36077341
DOID:0060929	non-syndromic X-linked intellectual developmental disorder 111	MGI:2679449	Mus musculus (house mouse)	245450	Slitrk2		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:35840571
DOID:9351	diabetes mellitus	WB:WBGene00000898	Caenorhabditis elegans	175410	daf-2		combinatorial experimental and author inference evidence used in manual assertion evidence used in automatic assertion mutant phenotype evidence used in manual assertion	MGI:6194238 PMID:35729173
DOID:684	hepatocellular carcinoma	HGNC:4057	Homo sapiens (human)	2539	G6PD		evidence used in automatic assertion expression pattern evidence used in manual assertion	MGI:6194238 PMID:35693827
DOID:0070055	Xia-Gibbs Syndrome	MGI:2444218	Mus musculus (house mouse)	230793	Ahdc1		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:35585237
DOID:0080240	non-syndromic X-linked intellectual disability 106	FB:FBgn0261403	Drosophila melanogaster (fruit fly)	35486	sxc	CG10392	combinatorial experimental and author inference evidence used in manual assertion combinatorial experimental and curator inference evidence used in manual assertion evidence used in automatic assertion	MGI:6194238 PMID:35500025 PMID:37286164
DOID:0110295	autosomal recessive limb-girdle muscular dystrophy type 2U	MGI:1923097	Mus musculus (house mouse)	75847	Crppa		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:35422047
DOID:0081168	HMG-CoA synthase 2 deficiency	MGI:101939	Mus musculus (house mouse)	15360	Hmgcs2		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:35421611
DOID:12120	pulmonary alveolar proteinosis	MGI:1339754	Mus musculus (house mouse)	12982	Csf2ra		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:35043685
DOID:0111814	methylmalonic acidemia and homocysteinemia cblX type	MGI:105942	Mus musculus (house mouse)	15161	Hcfc1		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:35013307
DOID:12802	mucopolysaccharidosis I	FB:FBgn0032343	Drosophila melanogaster (fruit fly)	34544	Idua		combinatorial experimental and author inference evidence used in manual assertion evidence used in automatic assertion	MGI:6194238 PMID:35011691
DOID:0110194	Charcot-Marie-Tooth disease type 4B3	MGI:1925230	Mus musculus (house mouse)	77980	Sbf1		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:34718573
DOID:1596	depressive disorder	FB:FBgn0011582	Drosophila melanogaster (fruit fly)	41726	Dop1R1		combinatorial experimental and author inference evidence used in manual assertion evidence used in automatic assertion	MGI:6194238 PMID:34654742
DOID:0080572	congenital disorder of glycosylation Iw	SGD:S000002990	Saccharomyces cerevisiae S288C	852862	STT3		evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:34653363
DOID:0070069	autosomal dominant intellectual developmental disorder 39	MGI:1100511	Mus musculus (house mouse)	17933	Myt1l		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:34614421 PMID:35538503
DOID:0112072	nuclear type mitochondrial complex I deficiency 20	MGI:1914272	Mus musculus (house mouse)	229211	Acad9		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:34556413
DOID:0110199	Charcot-Marie-Tooth disease dominant intermediate C	MGI:2147627	Mus musculus (house mouse)	107271	Yars1		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:34516839
DOID:0050629	Aicardi-Goutieres syndrome	MGI:1889575	Mus musculus (house mouse)	56417	Adar		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:34332594 PMID:34343497
DOID:0080698	Teebi hypertelorism syndrome 1	MGI:1921642	Mus musculus (house mouse)	74392	Specc1l		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:34302166
DOID:0110739	neurodegeneration with brain iron accumulation 5	MGI:1859606	Mus musculus (house mouse)	54636	Wdr45		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:34043061
DOID:14780	KBG syndrome	MGI:1924337	Mus musculus (house mouse)	77087	Ankrd11		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:33996804
DOID:0060227	Adams-Oliver syndrome	MGI:1859388	Mus musculus (house mouse)	54485	Dll4		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:33899511
DOID:0110567	autosomal dominant nonsyndromic deafness 41	MGI:2665170	Mus musculus (house mouse)	231602	P2rx2		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:33791800
DOID:0050431	arrhythmogenic right ventricular cardiomyopathy	ZFIN:ZDB-GENE-031116-55	Danio rerio (zebrafish)	560091	dsc2l		author statement supported by traceable reference used in manual assertion evidence used in automatic assertion	MGI:6194238 PMID:33784018
DOID:5408	Paget's disease of bone	MGI:1314891	Mus musculus (house mouse)	21934	Tnfrsf11a		author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:33724536

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