GlyCosmos Portal

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

Displaying entries **5826 - 5850** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:1586	rheumatic fever Aliases: ACUTE RHEUMATIC FEVER RhF - Rheumatic fever	Icam1	25464	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L Aliases: LGMD2L muscular dystrophy, limb-girdle, type 2L	Fktn	362520	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9279	hyperhomocysteinemia	ngfb	58133	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:1040	chronic lymphocytic leukemia Aliases: B-cell chronic lymphocytic leukaemia B-cell chronic lymphocytic leukemia CLL chronic lymphatic leukaemia chronic lymphatic leukemia chronic lymphocytic leukaemia lymphoplasmacytic leukaemia lymphoplasmacytic leukemia	Cd40lg Cd79b Cd86 Il5 Myc Pon1 Stat3	12524 15985 16191 17869 18979 20848 21947	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11725	Cornelia de Lange syndrome Aliases: Brachmann de Lange syndrome De Lange syndrome	NIPBL PDS5A SMC1A SMC3	23244 25836 8243 9126	Homo sapiens (human)	Alliance of Genome Resources
DOID:3179	inverted papilloma Aliases: Inverted papilloma, squamous cell	Hgf Kdr Vegfa	24446 25589 83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070046	Coffin-Siris syndrome 4 Aliases: CSS4 MRD16 autosomal dominant mental retardation 16	Smarca4	20586	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1573	communicating hydrocephalus	Tmem67	329795	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14761	Greig cephalopolysyndactyly syndrome Aliases: polysyndactyly with peculiars skull shape	GLI3	2737	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080858	primary ovarian insufficiency 2A	BNI1	855450	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13714	anodontia Aliases: Complete absence of teeth Developmental absence of tooth Total anodontia of permanent and deciduous teeth	W01F3.2 zmp-3 zmp-4	178748 179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080263	autosomal recessive nonsyndromic deafness 108	Ror1	26563	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13372	alpha 1-antitrypsin deficiency Aliases: AAT deficiency	serpine3	556612	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0111292	idiopathic generalized epilepsy 10 Aliases: EIG10	Lcch3	32554	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050741	alcohol dependence Aliases: alcoholism	ADH1B ADH1C ADH4 ADRA2A AGO1 AGO2 AHR ALDH2 ANGPT1 AR BDNF BMAL1 BPTF CACNA1C CCK CHRNA3 CHRNB3 COMT CPE CREB1 CYP2C9 CYP2E1 CYP3A5 DRD1 DRD2 DRD4 FMN1 FOS FOSB GABBR1 GABRA2 GABRB3 GABRG2 GAD1 GAD2 GDNF GEMIN4 GGT1 GGTLC1 GGTLC2 GRIN2A GRM8 HTR1A HTR1B HTR2A HTR3A IGF1R IL1RN INSR INSRR KCNB2 LEP NCAM1 NGF NGFR NR3C2 NRXN3 NUCB2 OPRD1 OPRK1 OPRM1 PDE4B PER2 POMC PRL RPS6KB1 SLC29A1 SLC6A1 SLC6A2 SLC6A4 TAS2R16 XRCC5	1136 1142 125 126 127 1312 1363 1385 150 1559 1571 1577 1812 1813 1815 196 2030 217 2186 2353 2354 2550 2555 2562 2566 2571 2572 26523 2668 2678 27161 284 2903 2918 3350 3351 3356 3359 342184 3480 3557 3643 3645 367 3952 406 4306 4684 4803 4804 4925 4985 4986 4988 50628 50833 5142 5443 5617 6198 627 6529 6530 6532 7520 775 885 8864 91227 92086 9312 9369	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110969	brachydactyly type B1 Aliases: BDB1	cam-1	174473	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060318	acute promyelocytic leukemia Aliases: acute myeloblastic leukaemia type 3 acute myeloblastic leukemia type 3 acute myeloid leukaemia M3 acute myeloid leukemia M3 acute promyelocytic leukaemia	myca mycb	30686 393141	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0080181	PHARC syndrome Aliases: polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract	abhd12	100216158	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:525	central nervous system vasculitis	HLA-A	3105	Homo sapiens (human)	Alliance of Genome Resources
DOID:0040085	bacterial sepsis	TREM1	54210	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110351	osteogenesis imperfecta type 11 Aliases: OI11 osteogenesis imperfecta type XI	FKBP10	60681	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110122	Axenfeld-Rieger syndrome type 3 Aliases: Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss RIEG3 Rieger syndrome type 3 anterior chamber cleavage syndrome anterior segment mesenchymal dysgenesis	BMP4 FOXC1	2296 652	Homo sapiens (human)	Alliance of Genome Resources
DOID:2316	brain ischemia Aliases: Ischaemic encephalopathy Ischemic encephalopathy cerebral ischemia	CDC25 MDH1 MDH2 MDH3 SMF3 STE20 STE6	850721 851019 851481 853671 853777 853994 856382	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060447	epithelial basement membrane dystrophy Aliases: Cogan corneal dystrophy EBMD microcystic corneal dystrophy	YLR001C	850687	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110248	cataract 30 Aliases: CTRCT30 Dusty cataract cataract 30 pulverulent cataract Coppock-like	Vim	22352	Mus musculus (house mouse)	Alliance of Genome Resources

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