GlyCosmos Portal

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

Displaying entries **5751 - 5775** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0060717	autosomal recessive congenital ichthyosis 8 Aliases: ARCI8 lamellar ichthyosis 4 late-onset lamellar ichthyosis	lipl-1 lipl-2 lipl-3 lipl-4 lipl-5	178563 178572 179046 179771 185840	Caenorhabditis elegans	Alliance of Genome Resources
DOID:6846	familial melanoma	Braf Mc1r Mitf	109880 17199 17342	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2739	Gilbert syndrome Aliases: Constitutional hyperbilirubinemia Gilbert's disease Gilbert's syndrome Gilbert-Meulengracht syndrome hereditary nonhemolytic jaundice	ugt-61	185500	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10772	thrombotic thrombocytopenic purpura Aliases: Moschcowitz's syndrome	scav-2 scav-3	176673 176787	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110195	Charcot-Marie-Tooth disease type 4E Aliases: CMT4E Charcot-Marie-Tooth neuropathy type 4E Neuropathy, congenital hypomyelinating, 1 autosomal recessive congenital hypomyelinating or amyelinating neuropathy	EGR2	1959	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080019	metaphyseal dysplasia Aliases: Bakwin-Krida syndrome Pyle's disease Pyle-Cohn syndrome	Sfrp4	20379	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13148	acute cystitis	Lcn2	170496	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3443	mammary Paget's disease Aliases: Paget cell neoplasm Paget's disease Paget's disease of the breast mammary Paget disease	Egfr	37455	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111819	syndactyly type 5 Aliases: SDTY5 syndactyly with associated metacarpal and metatarsal fusion	HOXD13	3239	Homo sapiens (human)	Alliance of Genome Resources
DOID:10825	essential hypertension Aliases: idiopathic hypertension primary hypertension	Add1 Agtr1a Agtr1b Atp1b1 Atp5pf Fgfr2 Havcr1 Hsd11b1 Lcn2 Nos3 Npr2 Rbp4 Ren Slc12a3 Timd2	116564 170496 24170 24180 24600 24715 25022 25116 25650 25703 286934 287222 54300 81638 94271	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060482	oculoauricular syndrome	HMX1	3166	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060419	chromosome 3q29 microdeletion syndrome Aliases: 3q subtelomere deletion syndrome 3q29 microdeletion syndrome 3q29 recurrent deletion 3qter deletion	slc51a	447807	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110025	age related macular degeneration 13 Aliases: ARMD13	Cfi	79126	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111346	epidermolysis bullosa simplex with mottled pigmentation Aliases: EBSMP Epidermolysis bullosa simplex-MP speckled hyperpigmentation with punctate palmoplantar keratoses and childhood blistering	Krt5	369017	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111239	congenital muscular dystrophy-dystroglycanopathy type A10 Aliases: MDDGA10 Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10	Rxylt1	216395	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1184	nephrotic syndrome	A2M ACAT1 ACE ALB ALOX5 APOA1 APOB APOC2 APOC3 APOE CD2AP CFI CFL1 COQ2 COQ6 CPB2 CTSL CTSV DGAT1 ECE1 EDNRA EPO FAT1 GAPVD1 GP1BA GPAM GPX1 GPX3 IGFALS IL1RN IL4 IL5 ITSN2 KCNJ1 KIRREL1 KIRREL2 KIRREL3 LIPC NOS1 NPHS1 NPHS2 NR3C1 PLA2G7 PLCE1 PPARGC1A PTGS2 SCNN1A SCNN1B SERPINC1 SGPL1 SH3KBP1 SOAT2 SOD2 STOM TFPI TNFRSF11B VLDLR	1072 10891 1361 1514 1515 1636 1889 1909 2 2040 2056 213 2195 23607 240 26130 27235 2811 2876 2878 2908 30011 335 338 3426 344 345 348 3483 3557 3565 3567 3758 38 3990 462 4842 4868 4982 50618 51004 51196 55243 5743 57678 6337 6338 6648 7035 7436 7827 7941 84063 8435 84623 8694 8879	Homo sapiens (human)	Alliance of Genome Resources
DOID:8634	prostate carcinoma in situ Aliases: PIN III carcinoma in situ of prostate grade III PIN	Areg Aurkb Carm1 Creb3l4 Csf1r Esr1 Esr2 Fgf6 Fgf8 Flt1 Fzd4 Hdac1 Lrp1 Map2k4 Phb1 Prss8 Ptgs2 Rela Rxra Smad4 St14	11839 12978 13982 13983 14177 14179 14254 14366 16971 17128 18673 19143 19225 19697 20181 20877 26398 433759 59035 76560 78284	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080425	developmental and epileptic encephalopathy 47 Aliases: DEE47 early infantile epileptic encephalopathy 47	Fgf10 Fgf16 Fgf5 Fgf6 Fgf7	14165 14176 14177 14178 80903	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060698	hyperekplexia 3 Aliases: HKPX3	Slc6a5	171148	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3138	acanthosis nigricans Aliases: keratosis nigricans	VVS1	852543	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070170	spermatogenic failure 19 Aliases: SPGF19	CFAP43	80217	Homo sapiens (human)	Alliance of Genome Resources
DOID:3490	Noonan syndrome Aliases: Turner's phenotype, karyotype normal	enok	37859	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080771	beta-thalassemia major Aliases: Cooley's anemia	Pon1	18979	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110409	retinitis pigmentosa 46 Aliases: RP46	IDH3B	3420	Homo sapiens (human)	Alliance of Genome Resources
DOID:848	arthritis Aliases: Inflammatory disorder of joint	Cnr2 Fcgr3a Parp1 Tlr4	25591 29260 304966 57302	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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