GlyCosmos Portal

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

Displaying entries **12976 - 13000** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:9074	systemic lupus erythematosus Aliases: Lupus Erythematosus, systemic SLE - Lupus Erythematosus, systemic disseminated lupus erythematosus	C1qa C3 C4a Ccl2 Ccr5 Cd40lg Cd46 Clu Crp Cxcr2 Cyp1a1 Dnase1 Esr2 Fas Fcgr2a Fcgr2al1 Fcgr2b Fcgr3a Hspd1 Ifng Il10 Il13 Il1rn Il21 Il2 Ldlr Man2a1 P2ry12 Pgf Pparg Ptprc Sell Sftpd Slc11a1 Sod2 Tfpi Tnf Tnfrsf1a Tnfrsf1b Vcam1 Vim	116553 116562 116591 117029 156767 24232 24233 24296 246097 24699 24770 24787 24835 24854 25149 25325 25350 25361 25419 25478 25625 25633 25664 25712 289211 29259 29333 29385 29436 298566 300438 304966 316519 365769 498276 60582 63868 64803 81818 84349 94203	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	C1galt1c1	59048	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	C1galt1c1 Ccl2 Cd36 Cd46 Cfh Cfhr4 F2 Hp Il1rl1 Il1rn Mbl2 Pla2g7 Plat	12491 12628 14061 15439 16181 17082 17195 17221 18791 20296 214403 27226 59048	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	C1galt1c1	302499	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	C1galt1c1 Ccl2 Cd46 Hp Il1rl1 Il1rn Plat	24464 24770 25556 25692 29333 302499 60582	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060050	autoimmune disease of blood	C1galt1	94192	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060050	autoimmune disease of blood	C1galt1	65044	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080987	Ehlers-Danlos syndrome periodontal type 2	C1S	716	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080986	Ehlers-Danlos syndrome periodontal type 1	C1R	715	Homo sapiens (human)	Alliance of Genome Resources
DOID:37	skin disease Aliases: Genodermatosis skin and subcutaneous tissue disease	C1QTNF9 IL10 OTOL1 TNF	131149 338872 3586 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111495	combined oxidative phosphorylation deficiency 33 Aliases: COXPD33	C1QBP	708	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060050	autoimmune disease of blood	C1GalTA	34215	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	C1GALT1C1	29071	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	C1GALT1C1 CCL2 CD36 CD46 CFH F2 HP IL1RL1 IL1RN MBL2 PLA2G7 PLAT	2147 29071 3075 3240 3557 4153 4179 5327 6347 7941 9173 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060050	autoimmune disease of blood	C1GALT1	56913	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112209	developmental and epileptic encephalopathy 73 Aliases: DEE73 early infantile epileptic encephalopathy 73	C18B12.4	181600	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110593	autosomal dominant nonsyndromic deafness 9 Aliases: DFNA9 autosomal dominant deafness 9	C16E9.1	182693	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	C16D9.6	182687	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	C16D9.6 scav-2 scav-3	176673 176787 182687	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050667	alcohol-related neurodevelopmental disorder Aliases: ARND static encephalopathy	C15H9.4	182643	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111042	glycogen storage disease IXa Aliases: GSD type 9A GSD type IXa GSD9A glycogen storage disease type 9A glycogen storage disease type IXa glycogenosis type 9A glycogenosis type IXa	C14B9.8	176149	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111040	glycogen storage disease IXd Aliases: GSD IXd GSD due to muscle phosphorylase kinase deficiency GSD type 9D GSD type 9E GSD type IXd GSD type IXe GSD9D X-linked muscke glycogenosis glycogen storage disease due to muscle phosphorylase kinase deficiency glycogen storage disease type 9D glycogen storage disease type 9E glycogen storage disease type IXd glycogen storage disease type IXe glycogenosis due to muscle phosphorylase kinase deficiency glycogenosis type 9D glycogenosis type 9E glycogenosis type IXd glycogenosis type IXe muscle phosphorylase kinase deficiency	C14B9.8	176149	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2747	glycogen storage disease Aliases: glycogenosis	C14B9.8 gsy-1 gyg-2 pfk-1.1 pfk-1.2	174924 176149 179335 180119 180583	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050545	visceral heterotaxy Aliases: heterotaxia situs ambiguus	C14B9.8 daf-4 kpc-1	173051 175781 176149	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1459	hypothyroidism Aliases: Thyroid deficiency Thyroid insufficiency	C14B9.8 W01C8.5 bli-3 cts-1 cwn-1 daf-7 duox-2 gpx-3 gpx-5 grd-2 lad-2 ncam-1 pbo-4 pgal-1 wrt-6	171608 172108 173399 175237 176149 176437 177078 180349 180418 180638 180836 181178 181285 182513 186188	Caenorhabditis elegans	Alliance of Genome Resources

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