GlyCosmos Portal

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Alliance of Genome Resources	July 29, 2024
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Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **6201 - 6225** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:3319	lymphangioleiomyomatosis Aliases: lung lymphangioleiomyomatosis lymphangiomyomatosis pulmonary lymphangioleiomyomatosis	Cpt1a Gapdh	24383 25757	Rattus norvegicus (Norway rat)
DOID:12382	complex partial epilepsy Aliases: Complex partial epileptic seizure epilepsy, psychomotor psychomotor epilepsy	ACE ACOT7 ENO2 EPHX2 GAD1 GAD2 GLUL ICAM1 MGAT1 MICA PLD1 PLD2 PRNP PTGS2 RGMA SC5D SEMA7A SMUG1	100507436 11332 1636 2026 2053 23583 2571 2572 2752 3383 4245 5337 5338 5621 56963 5743 6309 8482	Homo sapiens (human)
DOID:4001	ovarian carcinoma	Akt2	25233	Rattus norvegicus (Norway rat)
DOID:0110543	autosomal dominant nonsyndromic deafness 11 Aliases: DFNA11 autosomal dominant deafness 11	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)
DOID:12384	dysentery Aliases: Infectious diarrhea	ACOT7 APRT IL18R1 LCT LYZ SULT1E1	11332 353 3938 4069 6783 8809	Homo sapiens (human)
DOID:3410	carotid artery thrombosis	ACE ARSA ART4 CD14 CD74 CHIT1 CYP2C19 FCGR3B KL LIPC LPL PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 SACM1L SMUG1 ST8SIA4 TM7SF2 VCAM1	1118 1557 1636 2215 22908 23583 3990 4023 410 420 5130 5290 5291 5293 5294 7108 7412 7903 7941 929 9365 972	Homo sapiens (human)
DOID:0081292	traumatic brain injury	Bad Trp53	12015 22059	Mus musculus (house mouse)
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	cht-1	180628	Caenorhabditis elegans
DOID:0110551	autosomal dominant nonsyndromic deafness 21 Aliases: DFNA21 autosomal dominant deafness 21	ACO2 ACOX1 ARSA CD109 CHSY1 COG4 LRTOMT OTOA OTOG PSAP TECTA	135228 146183 220074 22856 25839 340990 410 50 51 5660 7007	Homo sapiens (human)
DOID:0090026	split hand-foot malformation 6 Aliases: SHFM6	QTRT1 UGT8	7368 81890	Homo sapiens (human)
DOID:0014667	disease of metabolism Aliases: metabolic disease	Ldh Pfk PyK	36060 42620 45880	Drosophila melanogaster (fruit fly)
DOID:2377	multiple sclerosis Aliases: Generalized multiple sclerosis insular sclerosis	b4galt5.L b4galt5.S b4galt6.L b4galt6.S	108695277 108702589 446703 779435	Xenopus laevis (African clawed frog)
DOID:0050647	Arts syndrome Aliases: ARTS Lethal ataxia with deafness and optic atrophy MRXS18 MRXSARTS fatal X-linked ataxia with deafness and loss of vision syndromic X-linked mental retardation 18 syndromic X-linked mental retardation Arts type	PRPS1	5631	Homo sapiens (human)
DOID:10590	mild pre-eclampsia	GPX3	2878	Homo sapiens (human)
DOID:0060227	Adams-Oliver syndrome Aliases: Adams Oliver syndrome	eogt.L	443983	Xenopus laevis (African clawed frog)
DOID:1474	aggressive periodontitis Aliases: juvenile periodontitis	ALOX5 CD14 CYP1A1 DGKA FCGR3B GLT6D1 IL1R1 MBL2 MMP25 PAFAH1B1 PTGS2 SELE SIGLEC5 SMPD3 VCAM1	1543 1606 2215 240 3554 360203 4153 5048 55512 5743 6401 64386 7412 8778 929	Homo sapiens (human)
DOID:3055	paratyphoid fever Aliases: Paratyphoid Paratyphoid A fever Paratyphoid B fever Paratyphoid C fever Paratyphoid fever A Paratyphoid fever B Paratyphoid fever C paratyphoid a paratyphoid b paratyphoid c	ABO CD38	28 952	Homo sapiens (human)
DOID:0111135	congenital generalized lipodystrophy type 1 Aliases: Berardinelli-Seip Congenital Lipodystrophy, Type 1 Brunzell syndrome AGPAT2-related	AGL AGPAT1 AGPAT2 AGPS ATP6V0A2 ATP6V1A B4GALT7 CD38 DDOST DOLK FKTN FUCA1 GPC3 LPIN1 LPIN2 LPL PARP2 PCK1 PCYT1A PIK3CA PIK3CB PIK3CD PIK3CG PMM2 PNPLA2 SCD SDHA SMUG1 XYLT2	10038 10554 10555 11285 1650 178 2218 22845 23175 23545 23583 2517 2719 4023 5105 5130 523 5290 5291 5293 5294 5373 57104 6319 6389 64132 8540 952 9663	Homo sapiens (human)
DOID:0080470	developmental and epileptic encephalopathy 36 Aliases: congenital disorder of glycosylation, type Is early infantile epileptic encephalopathy 36	ALG13	852835	Saccharomyces cerevisiae S288C
DOID:10140	dry eye syndrome Aliases: Tear film insufficiency dry eye disease	Tlr4	29260	Rattus norvegicus (Norway rat)
DOID:0050729	Chanarin-Dorfman syndrome Aliases: neutral lipid storage disease	AGK CPT2 DGAT1 LPIN2 PEMT PNPLA2 PNPLA3	10400 1376 55750 57104 80339 8694 9663	Homo sapiens (human)
DOID:7079	adult cystic teratoma	ALPP DHCR24 FMOD GFRA1 PSMD10 PTEN	1718 2331 250 2674 5716 5728	Homo sapiens (human)
DOID:0060470	salt and pepper syndrome Aliases: salt & pepper syndrome salt-and-pepper syndrome	st3gal5	394230	Danio rerio (zebrafish)
DOID:1561	cognitive disorder Aliases: cognitive disease	Comt	12846	Mus musculus (house mouse)
DOID:0050742	nicotine dependence Aliases: tobacco use disorder	ACAN ACE ADH1C ADH7 AKR1A1 AKR1B10 ARSD BDH1 CACNA2D3 CDH13 CHAT COMT CYP21A2 CYP2B6 CYP2E1 CYP3A5 DGKG EFNA5 GALNTL6 GM2A HPGDS HS6ST3 HSD17B3 HTR2A MACROD1 MGAT4C NAAA NCAM1 NPY1R NTM OPCML PCCA PIGC PIK3CB PLA2G4E PLA2G6 PLCB1 PLCB4 PNPLA2 PTEN SLC39A8 XXYLT1	1012 10327 1103 123745 126 131 1312 152002 1555 1571 1577 1589 1608 1636 176 1946 23236 25834 266722 27163 27306 2760 28992 3293 3356 414 442117 4684 4886 4978 50863 5095 5279 5291 5332 55799 57016 57104 5728 622 64116 8398	Homo sapiens (human)

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