GlyCosmos Portal

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

Displaying entries **5351 - 5375** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:9883	Becker muscular dystrophy Aliases: Benign pseudohypertrophic muscular dystrophy benign congenital myopathy	DMD	1756	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112307	sarcosinemia Aliases: SARCOS SARD deficiency SARDH deficiency demethylation defect of N-methylglycine sarcosine dehydrogenase complex deficiency	SARDH	1757	Homo sapiens (human)	Alliance of Genome Resources
DOID:14323	Marfan syndrome Aliases: Marfan's syndrome	W01F3.2 cri-2 daf-4 dbl-1 fbn-1 mua-3 timp-1 zmp-3 zmp-4	175781 176076 176430 178748 179068 179197 179199 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:219	colon cancer	F47E1.2 R193.2 cwn-2 daf-4 gpx-3 gpx-5 hst-3.2 plr-1 zmp-3	175781 176575 177870 178748 181145 181178 182256 182513 3564879	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2920	membranoproliferative glomerulonephritis Aliases: Lobular glomerulonephritis chronic glomerulonephritis, lobular	C49C8.5 Y43C5A.2 cof-2 daf-4 ost-1	175781 176931 177668 177911 183582	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4762	vasculogenic impotence	C49C8.5 Y43C5A.2 daf-4	175781 177668 177911	Caenorhabditis elegans	Alliance of Genome Resources
DOID:11198	DiGeorge syndrome Aliases: 22q11.2 deletion syndrome DiGeorge sequence DiGeorge's syndrome Pharyngeal pouch syndrome	daf-4 hst-1	175781 177675	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112182	mismatch repair cancer syndrome Aliases: BTP1 syndrome BTPS1 CMMR-D syndrome CMMRDS MMR deficiency Turcot syndrome brain tumor-polyposis syndrome 1 childhood cancer syndrome constitutional mismatch repair deficiency syndrome	daf-4 rnst-2	175781 190096	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070234	Loeys-Dietz syndrome 2 Aliases: AAT3 LDS2 Marfan syndrome type II familial throacic aortic aneurysm 3	daf-4	175781	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110214	cleft soft palate Aliases: cleft velum cleft velum palatinum soft cleft palate	daf-4	175781	Caenorhabditis elegans	Alliance of Genome Resources
DOID:4258	Weissenbacher-Zweymuller syndrome Aliases: Piere-Robin syndrome Pierre Robin Malformation	daf-4	175781	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070273	hereditary nonpolyposis colorectal cancer type 6 Aliases: HNPCC6	daf-4	175781	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060856	right atrial isomerism Aliases: Ivemark syndrome asplenia with cardiovascular anomalies	daf-4	175781	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050949	autosomal recessive hypophosphatemic rickets	DMP1	1758	Homo sapiens (human)	Alliance of Genome Resources
DOID:5154	borna disease Aliases: Enzootic encephalomyelitis	aldo-1 aldo-2 parg-1 parg-2 parp-1	175827 176788 177683 186765 266823	Caenorhabditis elegans	Alliance of Genome Resources
DOID:438	autoimmune disease of the nervous system	aldo-1 aldo-2	175827 176788	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112201	osteogenesis imperfecta type 21 Aliases: OI21 osteogenesis imperfecta type XXI	erd-2.2	175833	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080572	congenital disorder of glycosylation Iw Aliases: congenital disorder of glycosylation 1w	stt-3	175886	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080573	congenital disorder of glycosylation Ix Aliases: congenital disorder of glycosylation 1x	stt-3	175886	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111223	centronuclear myopathy 1 Aliases: CNM1	DNM1 DNM2 MTMR14	1759 1785 64419	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B Aliases: CMTDI1 CMTDIB Charcot-Marie-Tooth neuropathy dominant intermediate B DI-CMTB	DNM1 DNM2	1759 1785	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070376	developmental and epileptic encephalopathy 31B Aliases: DEE31B	DNM1	1759	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080437	developmental and epileptic encephalopathy 31A Aliases: DEE31 DEE31A developmental and epileptic encephalopathy 31 early infantile epileptic encephalopathy 31	DNM1	1759	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080563	congenital disorder of glycosylation Ik Aliases: congenital disorder of glycosylation 1k	algn-1	175920	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3454	brain infarction	W01F3.2 cpr-3 cpr-4 cpr-6 parg-1 parg-2 pcp-1 pdfr-1 twk-46 unc-36 zmp-3 zmp-4	175942 176086 176155 177683 178748 179053 179991 180033 180252 180351 180931 186765	Caenorhabditis elegans	Alliance of Genome Resources

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