GlyCosmos Portal

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

Displaying entries **5626 - 5650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:4195	hyperglycemia	ADRB1 AKR1B1 AVP CBL CCL11 CYP11A1 CYP2C9 DRD1 EPAS1 F2 F7 GCK GIPR GLP1R GPX1 HCRTR2 HK2 HK3 HKDC1 HP HRH3 HSPD1 HSPG2 HTR2A ICAM1 IL1A IL1RN IL6 ITGAM ITGAV LDHA LEPR MMP9 PCSK1 PDX1 PKLR PLA2G4A PON1 PPARGC1A PRNP PTCH1 SDC1 SOD1 TF TSHB	10891 11255 153 1559 1583 1812 2034 2147 2155 231 2645 2696 2740 2876 3062 3099 3101 3240 3329 3339 3356 3383 3552 3557 3569 3651 3684 3685 3939 3953 4318 5122 5313 5321 5444 551 5621 5727 6356 6382 6647 7018 7252 80201 867	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070067	White-Sutton syndrome Aliases: MRD37 WHSUS autosomal dominant mental retardation 37	POGZ	23126	Homo sapiens (human)	Alliance of Genome Resources
DOID:5052	melioidosis Aliases: Nightcliff gardener's disease Pseudoglanders Whitmore's disease acute and fulminating melioidosis subacute and chronic melioidosis	IRAK3 PLAUR SERPINF1 TLR5 TREM1	11213 5176 5329 54210 7100	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112133	severe congenital neutropenia 3 Aliases: Kostmann disease Kostmann syndrome SCN3 infantile agranulocytosis	HAX1	10456	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080333	aortic valve disease 1	ENPP1 IL6 NOTCH1	3569 4851 5167	Homo sapiens (human)	Alliance of Genome Resources
DOID:13207	proliferative diabetic retinopathy Aliases: PDR	ADIPOQ AGER BCOR CALD1 CALU CAT CCL2 CCN1 COL5A2 COL6A3 CORO1C ENPP2 FLT1 IL6R PDGFB PPARG PTPN1 RBP4 SERPINE1 SERPINF1 SLIT2 SRSF6 TIMM44 VEGFA	10469 1290 1293 177 2321 23603 3491 3570 5054 5155 5168 5176 5468 54880 5770 5950 6347 6431 7422 800 813 847 9353 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060787	hypomyelinating leukodystrophy 2 Aliases: HLD2 PMLD1 Pelizaeus-Merzbacher-like disease 1 Pelizaeus-Merzbacher-like disease due to GJC2 mutation	GJC2	57165	Homo sapiens (human)	Alliance of Genome Resources
DOID:480	movement disease	DRD2 EFNB3	1813 1949	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050590	severe congenital neutropenia	CSF3R ELANE HAX1	10456 1441 1991	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070422	syndromic X-linked intellectual disability Pilorge type Aliases: MRXSP	GLRA2	2742	Homo sapiens (human)	Alliance of Genome Resources
DOID:11994	atrophy of testis	BRCA2	675	Homo sapiens (human)	Alliance of Genome Resources
DOID:3774	chordoid glioma Aliases: Chordoid glioma of 3rd Ventricle Chordoid glioma of third ventricle third ventricle chordoid glioma	PRKCA	5578	Homo sapiens (human)	Alliance of Genome Resources
DOID:3114	serous cystadenocarcinoma Aliases: serous adenocarcinoma serous carcinoma	LHCGR TP53 XPC	3973 7157 7508	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080584	autosomal dominant Wolfram syndrome	WFS1	7466	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080317	megalencephalic leukoencephalopathy with subcortical cysts 2B Aliases: megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation	HEPACAM	220296	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110709	hypotrichosis 12 Aliases: Hypt12	RPL21	6144	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110782	hereditary spastic paraplegia 31 Aliases: SPG31 autosomal dominant spastic paraplegia 31 autosomal dominant spastic paraplegia type 31	REEP4	80346	Homo sapiens (human)	Alliance of Genome Resources
DOID:3181	oligodendroglioma Aliases: oligodendroglial neoplasm oligodendroglial tumor	EGF MGMT PTGES3 RB1	10728 1950 4255 5925	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060835	isolated microphthalmia 6 Aliases: MCOP6 posterior nonsyndromic microphthalmia	PRSS56	646960	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070296	primary autosomal recessive microcephaly Aliases: MCPH	ASPM DYNC1I2 KIF14 KNL1 LMNB1 LMNB2 NCAPD2 NCAPD3 PDCD6IP TRAPPC14 WDR62	10015 1781 23310 259266 284403 4001 55262 57082 84823 9918 9928	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080281	schizophrenia 19	RBM12	10137	Homo sapiens (human)	Alliance of Genome Resources
DOID:8970	subacute sclerosing panencephalitis Aliases: Immunosuppressive measles encephalitis Van Bogaert's sclerosing leukoencephalitis subacute sclerosing leukoencephalopathy	ACE IFNL1	1636 282618	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070151	hereditary sensory and autonomic neuropathy type 6 Aliases: HSAN6 hereditary sensory and autonomic neuropathy type VI	DST	667	Homo sapiens (human)	Alliance of Genome Resources
DOID:870	neuropathy Aliases: peripheral neuropathy	CTSS MPZ NEMF NRG1 YARS1	1520 3084 4359 8565 9147	Homo sapiens (human)	Alliance of Genome Resources
DOID:11151	cholecystolithiasis	PLA2G2A UGT1A1	5320 54658	Homo sapiens (human)	Alliance of Genome Resources

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