GlyCosmos Portal

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

Displaying entries **1376 - 1400** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0110849	xeroderma pigmentosum group G Aliases: XP group G XP7 XPG xeroderma pigmentosum VII	ERCC5	2073	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080030	spondyloepimetaphyseal dysplasia, Missouri type	Mmp13	17386	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070093	schizophrenia 18 Aliases: Chromosome 7q36.3 Duplication Syndrome, 362-Kb SCZD18	Slc1a1	20510	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:423	myopathy	Actb Clcn2 Clcnka Clcnkb Col15a1 Col18a1 Col4a1 Col4a2 Col4a3 Col4a4 Dnm2 Flnb Flnc Hmgcr Hnrnpa1 Hnrnpa3 Ldb3 Lmna Lmnb1 Lmnb2 Megf10 Megf11 Mtmr1 Myh13 Myh1 Myh2 Myh3 Myh4 Myh6 Myh7 Myh7b Pdlim5 Pdlim7 Pear1 Psmc5	11461 12724 12733 12819 12822 12826 12827 12828 12829 13430 140781 15357 15382 16905 16906 16907 17879 17882 17883 17884 17888 19184 214058 229279 24131 286940 53332 544791 56365 56376 668940 67399 68794 70417 73182	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080422	Dravet syndrome Aliases: DEE6 DEE6A developmental and epileptic encephalopathy 6 developmental and epileptic encephalopathy 6A early infantile epileptic encephalopathy 6 severe myoclonic epilepsy of infancy	para	32619	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060805	Prieto syndrome Aliases: Prieto-Badia-Mulas syndrome X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome	WNK3	65267	Homo sapiens (human)	Alliance of Genome Resources
DOID:1214	tympanosclerosis	Enpp1 Tlr4	29260 85496	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3611	acute retinal necrosis syndrome Aliases: acute retinal necrosis	Ifng	25712	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:670	amphetamine abuse	GluRIA	38742	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0112167	autosomal dominant nonsyndromic deafness 76 Aliases: DFNA76	PLS1	5357	Homo sapiens (human)	Alliance of Genome Resources
DOID:4481	allergic rhinitis Aliases: Non-seasonal allergic rhinitis Perenial allergic rhinitis atopic rhinitis hay fever pollenosis seasonal allergic rhinitis	pon1	447803	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:3319	lymphangioleiomyomatosis Aliases: lung lymphangioleiomyomatosis lymphangiomyomatosis pulmonary lymphangioleiomyomatosis	ACSS2 CPT1A ESR1 GAPDH GLS MMP9 NOS3 RICTOR SRF STAT1 STAT3 TSC1 TSC2	1374 2099 253260 2597 2744 4318 4846 55902 6722 6772 6774 7248 7249	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080365	endometrial hyperplasia	CA9 CDC25B JUP KRAS PTK2 SKP2 TFF1	3728 3845 5747 6502 7031 768 994	Homo sapiens (human)	Alliance of Genome Resources
DOID:14550	root resorption	Tnf Tnfrsf1a	24835 25625	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:11561	hypertensive retinopathy	Crp	25419	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110219	Brugada syndrome 2 Aliases: BRGDA2	Gpd1l	333433	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110206	Charcot-Marie-Tooth disease dominant intermediate F Aliases: CMTDIF autosomal dominant intermediate Charcot-Marie-Tooth disease type F	GNB4	59345	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110839	Usher syndrome type 2C Aliases: USH2C Usher syndrome IIC Usher syndrome type IIC	ADGRV1 PDZD7 SLC4A7	79955 84059 9497	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110074	arrhythmogenic right ventricular dysplasia 5 Aliases: ARVC5 ARVD5 arrhythmogenic right ventricular cardiomyopathy 5 familial arrhythmogenic right ventricular dysplasia 5	TMEM43	79188	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070294	primary autosomal recessive microcephaly 10 Aliases: MCPH10	Zfp335	329559	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050200	Korean hemorrhagic fever	Il2ra	25704	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112136	severe congenital neutropenia 4 Aliases: Dursun syndrome SCN4 autosomal recessive severe congenital neutropenia due to G6PC3 deficiency severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome	G6PC3	92579	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080546	non-alcoholic fatty liver Aliases: NAFL nonalcoholic fatty liver	Ggt1 Htr2a Htr2b Ngf	116568 29581 29595 310738	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111236	congenital muscular dystrophy-dystroglycanopathy type A3 Aliases: MDDGA3 Walker-Warburg syndrome or muscle-eye-brain disease, POMGNT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A3	Pomgnt1	362567	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080572	congenital disorder of glycosylation Iw Aliases: congenital disorder of glycosylation 1w	Stt3a Stt3b	363160 500972	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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