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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

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

Displaying entries **11301 - 11325** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:684	hepatocellular carcinoma Aliases: Hepatoma	C53D5.5 F47E1.2 T03D8.6 T13H5.8 W01A8.8 abt-2 acn-1 aldo-1 aldo-2 aprt-1 cest-1.2 cle-1 clec-88 cpl-1 cpr-3 cpr-4 cpr-6 daf-2 daf-4 ddr-2 dep-1 ges-1 gpx-3 gpx-5 gspd-1 hda-4 ire-1 lect-2 let-23 mrp-1 mrp-2 nep-2 pgp-1 pgp-3 plr-1 poml-1 poml-2 ptc-1 ptc-3 pxn-1 pxn-2 skn-1 stim-1 svh-2 ver-1 ver-4	171619 171782 171999 172232 172678 173631 173978 174056 174274 174305 174362 174437 174462 175182 175201 175410 175781 175827 176575 176788 177343 178046 178215 178633 179053 179914 180033 180111 180364 180408 180409 180622 180780 180929 180931 181145 181178 181288 181326 181723 182513 186632 187297 188090 191484 4926920	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9352	type 2 diabetes mellitus Aliases: NIDDM insulin resistance non-insulin-dependent diabetes mellitus type 2 diabetes type II diabetes mellitus	C27A7.3 C49C8.5 C53D5.5 F49B2.6 T03D8.6 W01C8.5 W01F3.2 W03G11.3 Y43C5A.2 abt-2 ace-1 ace-2 ace-3 acn-1 adm-4 aldo-1 anp-1 cht-1 cpd-2 cpi-1 cpl-1 cpr-3 cpr-4 cpr-6 cri-2 csq-1 daf-2 daf-4 dhrr-1 dop-2 dpf-1 dpf-2 egl-21 egl-3 enpp-1 fbn-1 gon-1 gpdh-3 gpx-3 gpx-5 gspd-1 klo-1 lev-9 mrp-1 mrp-7 ogt-1 parp-1 pbo-4 pgp-1 pgp-3 poml-1 poml-2 ptp-3 scav-1 scav-2 scav-3 sdn-1 skn-1 srp-1 srp-3 srp-7 ugt-22 ugt-26 ugt-62 ver-1 ver-4 zmp-2 zmp-3 zmp-4	171619 171782 171905 171999 172085 172509 173297 174685 175076 175182 175383 175410 175591 175781 176000 176076 176673 176787 176788 177343 177372 177557 177668 177850 177911 177940 178046 178215 178330 178585 178672 178748 179053 179195 179197 179347 179412 179663 179665 179763 179991 180033 180042 180111 180289 180351 180364 180409 180628 180780 180812 180836 180931 181041 181178 181259 181285 181326 181563 181579 181684 181706 182513 186632 187297 188252 189173 191374 266823	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1498	cholera Aliases: Cholera - Vibrio cholerae Cholera due to Vibrio cholerae Vibrio cholerae	bli-3 duox-2	171608 186188	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0112189	thyroid dyshormonogenesis 6 Aliases: TDH6 genetic defect in thyroid hormonogenesis 6	bli-3 duox-2	171608 186188	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050338	primary bacterial infectious disease	bli-3 duox-2 grd-1 grd-2 wrt-6	171608 180349 180638 181300 186188	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9281	phenylketonuria Aliases: Folling's disease PKU maternal phenylketonuria phenylalaninemia	bli-3 gspd-1	171608 178046	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050328	congenital hypothyroidism	bli-3 duox-2 gspd-1	171608 178046 186188	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
DOID:8778	Crohn's disease Aliases: Crohn disease Crohn's disease of colon Crohn's disease of large bowel Granulomatous Colitis Pediatric Crohn's disease	45566 R193.2 W01C8.5 acr-15 acr-16 acr-7 bli-3 dhrr-1 duox-2 eat-2 gpx-3 gpx-5 pgp-1 pgp-3 poml-1 poml-2 smf-1 smf-2 smf-3 ugt-61 ver-1 ver-4	171608 171999 172841 174262 175072 175182 177044 178215 179235 180836 180939 181178 181326 182256 182513 185500 186188 186632 187297 191374 191602 191766	Caenorhabditis elegans	Alliance of Genome Resources
DOID:8577	ulcerative colitis Aliases: Left-sided ulcerative colitis	R193.2 W01C8.5 acr-15 acr-16 acr-7 bli-3 cle-1 daf-2 dhrr-1 duox-2 eat-2 gpx-3 gpx-5 lev-9 pgp-1 pgp-3 poml-1 poml-2 smf-1 smf-2 smf-3 vab-1 ver-1 ver-4	171608 171999 172678 173794 174262 175072 175182 175410 177044 178215 179235 180836 180939 181178 181326 182256 182513 186188 186632 187297 188252 191374 191602 191766	Caenorhabditis elegans	Alliance of Genome Resources
DOID:3413	alpha-mannosidosis Aliases: Alpha-D-mannosidosis alpha-mannosidase deficiency deficiency of alpha-mannosidase	Man2b1	17159	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1338	congenital dyserythropoietic anemia Aliases: congenital dyshaematopoietic anaemia	Cdan1 Man2a1 Racgap1	17158 26934 68968	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060776	congenital diarrhea 5 with tufting enteropathy Aliases: DIAR5 congenital diarrhoea 5 with tufting enteropathy congenital familial intractable diarrhea with epithelial or epithelium abnormalities congenital familial intractable diarrhoea with epithelial or epithelium abnormalities congenital tufting enteropathy tufting enteropathy	Epcam	171577	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070270	hereditary nonpolyposis colorectal cancer type 8 Aliases: HNPCC8	Epcam	171577	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3565	meningioma Aliases: meningeal neoplasm meningothelial cell tumor neoplasm of the meninges primary Meningeal tumor	Hgf Spon2	171569 24446	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070460	hereditary spastic paraplegia 90B Aliases: SPG90B autosomal recessive spastic paraplegia 90B	SPTSSA	171546	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070459	hereditary spastic paraplegia 90A Aliases: SPG90A autosomal dominant spastic paraplegia 90A	SPTSSA	171546	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090076	hypogonadotropic hypogonadism 18 with or without anosmia	Il17rd	171463	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070047	Schuurs-Hoeijmakers Syndrome Aliases: MRD17 SHMS autosomal dominant mental retardation 17	Pacs1	171444	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111258	pentosuria Aliases: L-xylulose reductase deficiency L-xylulosuria PNTSU essential pentosuria xylitol dehydrogenase deficiency	Dcxr	171408	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:11612	polycystic ovary syndrome Aliases: Multicystic ovaries PCOS Polycystic Ovarian disease Polycystic ovaries Stein-Leventhal synd. Stein-Leventhal syndrome polycystic ovary	Adra1a Adra1d Adrb3 Akt2 Amh Atp5f1b Comt Cyp1a1 Fst Hsd17b7 Mmp2 Ngfr Pecam1 Serpine1 Th Vegfa	171374 24267 24296 24373 24596 24617 25085 25233 25378 25645 29412 29413 29540 29583 81686 83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080460	developmental and epileptic encephalopathy 34 Aliases: DEE34 early infantile epileptic encephalopathy 34	Slc12a5	171373	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111315	idiopathic generalized epilepsy 14 Aliases: EIG14	Slc12a5	171373	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110820	hereditary spastic paraplegia 75 Aliases: SPG75 autosomal recessive spastic paraplegia 75 autosomal recessive spastic paraplegia type 75	Mag	17136	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:573	nerve compression syndrome Aliases: Compression neuropathy entrapment neuropathy peripheral nerve entrapment syndrome	Mag	17136	Mus musculus (house mouse)	Alliance of Genome Resources

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