GlyCosmos Portal

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

Displaying entries **1276 - 1300** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:3594	choriocarcinoma Aliases: Chorioepithelioma	PHO8	852092	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080571	congenital disorder of glycosylation Iu Aliases: congenital disorder of glycosylation 1u	DPM2	8818	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111595	congenital contractural arachnodactyly Aliases: Beals syndrome Beals-Hecht syndrome CCA arachnodactyly, contractural Beals type contractures, multiple with arachnodactyly distal arthrogryposis type 9 ear anomalies-contractures-dysplasia of bone with kyphoscoliosis	Fbn2	14119	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11257	social phobia	CNTNAP2	26047	Homo sapiens (human)	Alliance of Genome Resources
DOID:4001	ovarian carcinoma	Akt2 Amh Ccr5 Il13 L1cam Vegfd	116553 117029 25233 25378 360457 50687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060224	atrial fibrillation Aliases: A-fib AFib	ACE AGER AGT AGTR1 ANK2 CAND2 CD36 CD40 EDN1 FLT1 GP6 HGF HIF1A IL2 ITGAM KCNE1 KCNE2 KCNJ5 KCNQ1 MMP1 MMP2 MMP3 MMP9 RBM20 REN ROBO1 SLC8A1 SLIT2 SOD1 TFPI TGFB1 TLR2 TNF TTN VEGFA VWF	1636 177 183 185 1906 23066 2321 282996 287 3082 3091 3558 3684 3753 3762 3784 4312 4313 4314 4318 51206 5972 6091 6546 6647 7035 7040 7097 7124 7273 7422 7450 9353 948 958 9992	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110985	Joubert syndrome 16 Aliases: JBTS16	tmem138	493444	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0050523	adult T-cell leukemia/lymphoma Aliases: Adult T-cell leukemia/lymphoma (HTLV-1 positive) adult T-cell leukemia	Fas Il10 Notch1	246097 25325 25496	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080561	congenital disorder of glycosylation Ii Aliases: congenital disorder of glycosylation 1i	ALG2	852815	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10322	berylliosis Aliases: beryllium poisoning	Btnl2 Ccr5 Tgfb1	12774 21803 547431	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080283	developmental and epileptic encephalopathy 55 Aliases: DEE55 GPIBD14 early infantile epileptic encephalopathy 55 glycosylphosphatidylinositol biosynthesis defect 14	Pigp	56176	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0014667	disease of metabolism Aliases: metabolic disease	CDC19 PFK1 PFK2 PYK2	851193 853155 854529 855245	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070397	hypomyelinating leukodystrophy 23 Aliases: HLD23	RNF220	55182	Homo sapiens (human)	Alliance of Genome Resources
DOID:2988	antiphospholipid syndrome Aliases: APS antiphospholipid antibody syndrome	APOH CCL5 CD40LG HLA-DQA1 HLA-DQB1 HLA-DRB1 PLAT PROC	3117 3119 3123 350 5327 5624 6352 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:13148	acute cystitis	Lcn2	16819	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111887	Diamond-blackfan anemia 3 Aliases: DBA3 RPS24-related Diamond-Blackfan anemia	RPS24	6229	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060246	MASA syndrome Aliases: CRASH syndrome Gareis-Mason syndrome L1 syndrome SPG1 X-linked complicated hereditary spastic paraplegia type 1 X-linked corpus callosum agenesis X-linked spastic paraplegia 1 hereditary spastic paraplegia 1	CHL1 L1CAM NFASC NRCAM TRPM1 TRPM3	10752 23114 3897 4308 4897 80036	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111818	syndactyly type 4 Aliases: Haas type syndactyly SDTY4 polysyndactyly, Haas type	SHH	6469	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112259	Leydig cell hypoplasia Aliases: 46,XY DSD due to LH resistance or LHB deficiency 46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency 46,XY disorder of sex development due to LH resistance or LHB deficiency 46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency	LHCGR	3973	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080558	congenital disorder of glycosylation If Aliases: congenital disorder of glycosylation 1f	mpdu1a mpdu1b	415220 447806	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:8553	pyoderma gangrenosum	MMP2 MMP9	4313 4318	Homo sapiens (human)	Alliance of Genome Resources
DOID:11949	Creutzfeldt-Jakob disease Aliases: CJD Creutzfeldt Jacob syndrome Creutzfeldt Jakob disease Creutzfeldt-Jacob disease Jakob-Creutzfeldt disease Subacute spongiform encephalopathy Transmissible virus dementia	Nefl Prnp Ptgs2 Serpina3c Serpina3n Snca	24686 24794 24795 29219 29527 83613	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:11830	myopia Aliases: near vision near-sightedness short-sightedness	col2a1	394828	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0111134	focal segmental glomerulosclerosis 9 Aliases: FSGS9	CRB2	286204	Homo sapiens (human)	Alliance of Genome Resources
DOID:3310	atopic dermatitis Aliases: Atopic neurodermatitis Besnier's prurigo allergic dermatitis atopic eczema	ADAM17 APOE BDNF C3 CCL28 CCR2 CCR3 CCR5 CD40 CDSN CLDN1 CMA1 CTLA4 CTSE CX3CL1 DOCK8 F2 FCGR2A HAVCR1 IFNG IL13 IL13RA1 IL13RA2 IL17A IL21R IL25 IL2 IL4 IL4R IL5 MBL2 NGF NGFR NTRK1 RELB SELP SHOC2 TGFB1 TLR2 TLR4 TNF TNFAIP6 TRAF3IP2 TSLP WASL	1041 10758 1215 1232 1234 1493 1510 2147 2212 26762 3458 348 3558 3565 3566 3567 3596 3597 3598 3605 4153 4803 4804 4914 50615 56477 5971 627 6376 6403 64806 6868 7040 7097 7099 7124 7130 718 729230 8036 81704 85480 8976 9076 958	Homo sapiens (human)	Alliance of Genome Resources

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