GlyCosmos Portal

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

Displaying entries **6851 - 6875** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0070232	benign recurrent intrahepatic cholestasis 2 Aliases: BRIC type 2 BRIC2	Abcb11	83569	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9427	hypertensive encephalopathy	BDNF PPARA	5465 627	Homo sapiens (human)	Alliance of Genome Resources
DOID:8947	diabetic retinopathy Aliases: Retinal abnormality - diabetes-related	ACE2 ACE ADIPOQ ADM ADRB3 AGER AGT AKR1B1 AKT1 ANGPT1 ANGPT2 AOC3 APOA4 APOB APOC3 APOE APOH AQP4 BDKRB1 BDNF CASP9 CAT CCL2 CCL5 CCN2 CD34 CD59 CDKAL1 CFB CFH CLDN1 CLU DLL4 EDN1 EGFR ELN ENG EP300 EPO F13A1 F3 F7 FLT1 FUCA1 GAPDH GC GGT1 GLO1 GLUL HFE HGF HIF1A HLA-B HLA-DQB1 HLA-DRB1 HRAS ICAM1 IGF1R IL10 IL1A IL6 INS INSR ITGA2 ITGA4 ITGAM ITGB3 KDM1A KEAP1 LTA MMP2 MMP9 NFE2L2 NGF NOS1 NOS3 NPPA NPR3 OCLN PDX1 PGF PIK3CG PON1 PPARGC1A PTEN RBP4 ROBO1 SERPINA4 SERPINE1 SERPINF1 SGF29 SLIT2 SOD1 SOD3 THBS1 TIMM44 TLR4 TNF VCAM1 VEGFA VPS26A VTN VWF WFS1 XRCC1	100506658 10469 10891 112869 1191 133 1490 155 1636 177 183 1906 1956 2006 2022 2033 2056 207 2152 2155 2162 23028 231 2321 2517 2597 2638 2678 2739 2752 284 285 3075 3077 3082 3091 3106 3119 3123 3265 337 338 3383 345 348 3480 350 3552 3569 3586 361 3630 3643 3651 3673 3676 3684 3690 4049 4313 4318 4780 4803 4842 4846 4878 4883 5054 5176 5228 5267 5294 5444 54567 54901 5728 59272 5950 6091 623 627 629 6347 6352 6647 6649 7057 7099 7124 7412 7422 7448 7450 7466 7515 842 847 8639 9076 9353 9370 947 9559 966 9817	Homo sapiens (human)	Alliance of Genome Resources
DOID:3069	malignant astrocytoma Aliases: Astrocytic tumor astrocytoma of Cerebrum astrocytoma of brain astroglioma cerebral astrocytoma	akt1.S akt2.L akt2.S	379783 399170 432172	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:1724	duodenal ulcer Aliases: Curling Ulcer Curling's ulcers Stress Ulcer	Cftr Slc11a2 Tfrc Vegfa	24255 25715 64678 83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111809	syndromic microphthalmia 2 Aliases: ANOP2 MAA2 MCOPS2 OFCD syndrome cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome microphthalmia cataracts radiculomegaly and septal heart defects oculofaciocardiodental syndrome syndromic microphthalmia type 2	BCOR	54880	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110033	autosomal recessive Alport syndrome	let-2	181708	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12351	alcoholic hepatitis Aliases: acute alcoholic hepatitis acute alcoholic liver disease	STE6	853671	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110680	congenital myasthenic syndrome 2C Aliases: CMS2C congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency	nAChRalpha1 nAChRalpha2 nAChRbeta2	42918 42919 42920	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050474	Netherton syndrome	GBA1	2629	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050565	autosomal recessive nonsyndromic deafness	tmtc4	560605	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0060071	pre-malignant neoplasm	ace smo	30225 565980	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0080537	hypermanganesemia with dystonia 2	SLC39A14	23516	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090068	giant axonal neuropathy 1	GAN	8139	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080562	congenital disorder of glycosylation Ij Aliases: Congenital disorder of glycosylation 1j	dpagt1	566539	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:2237	hepatitis Aliases: acute and subacute liver necrosis acute hepatitis acute/subac. necrosis of liver animal hepatitis chronic hepatitis chronic persistent hepatitis	ABO AFP ATP7B F5 GOLM1 IFNG LIPC NOS2 OGG1 PDCD1 SPP1 TF	174 2153 28 3458 3990 4843 4968 51280 5133 540 6696 7018	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110893	inflammatory bowel disease 13 Aliases: IBD13	Abcb1a Abcb1b	18669 18671	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080932	primary localized cutaneous amyloidosis 3 Aliases: Amyloidosis cutis dyschromica	GPNMB	10457	Homo sapiens (human)	Alliance of Genome Resources
DOID:11294	arteriovenous malformation Aliases: Arteriovenous hemangioma Cirsoid aneurysm Racemose Angioma Racemose aneurysm Racemose hemangioma	tek	30747	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0050642	hypochromic microcytic anemia	TNF	7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111808	linear skin defects with multiple congenital anomalies 1 Aliases: MCOPS7 MIDAS syndrome Microphthalmia with linear skin defect syndrome microphthalmia-dermal aplasia-sclerocornea syndrome syndromic microphthalmia 7 syndromic microphthalmia type 7	HCCS	3052	Homo sapiens (human)	Alliance of Genome Resources
DOID:11719	oculopharyngeal muscular dystrophy Aliases: Muscular dystrophy, oculopharyngeal	PABPN1	8106	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080217	lysosomal acid lipase deficiency Aliases: LAL deficiency LAL-D	Lipa	16889	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5517	stomach carcinoma Aliases: cancer of the stomach carcinoma of stomach gastric carcinoma	Egfr Kdm4B Parp1 btl htl	318918 3355109 37455 39564 42160	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4248	coronary stenosis Aliases: Coronary artery stenosis	Igf1r Pecam1 Tnfrsf11b	25341 25718 29583	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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