GlyCosmos Portal

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

Displaying entries **14951 - 14975** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:13619	extrahepatic cholestasis Aliases: extrahepatic biliary Stasis extrahepatic obstructive biliary disease	GIT1	850462	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5212	congenital disorder of glycosylation Aliases: carbohydrate-deficient glycoprotein syndrome	ALG1 ALG3 SEC53	850499 852196 852407	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050570	congenital disorder of glycosylation type I	ALG12 ALG1 ALG5 ALG6 ALG8 ALG9 DPM1 PMI40 RFT1 SEC53	850499 852261 852407 854163 854233 855502 855764 855874 856313 856720	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080552	congenital disorder of glycosylation Ia Aliases: PMM2-congenital disorder of glycosylation congenital disorder of glycosylation 1a	SEC53	850499	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050671	female breast cancer	RAD30 RIM15	850511 852028	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1588	thrombocytopenia	GAL10 LAS17 RIM15	850511 852307 854353	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111403	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations Aliases: MCCCHCM	RIM15	850511	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070394	developmental and epileptic encephalopathy 108 Aliases: DEE108 early infantile epileptic encephalopathy 108	RIM15	850511	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:4621	holoprosencephaly Aliases: Holoprosencephaly sequence	BST1 MCD4	850519 853690	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2747	glycogen storage disease Aliases: glycogenosis	GLG1 GPH1 GSY1 GSY2 PFK1 PFK2 VVS1	850569 850962 852543 853155 853932 855245 856289	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3534	Lafora disease Aliases: Lafora Progressive Myoclonic Epilepsy Lafora's disease MYOCLONIC EPILEPSY OF LAFORA	GSY1 GSY2	850569 850962	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:83	cataract	FAB1 GCY1 GLR1 HSF1 OGG1 SOR1 SOR2 VVS1 XYL2 YPR1 ZWF1	850574 850759 851351 851974 852543 852806 853624 854287 854942 855480 856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060448	Fleck corneal dystrophy Aliases: FCD Francois-Neetens speckled corneal dystrophy	FAB1	850574	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3070	high grade glioma Aliases: Neuroglial tumor glial cell tumor glioma, malignant malignant Neuroglial tumor malignant glioma	IDP1 IDP2 IDP3 IRC5 KAR2 STE6	850599 850871 851493 853418 853671 855723	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0090011	immunodeficiency-centromeric instability-facial anomalies syndrome 4 Aliases: ICF syndrome 4	IRC5	850599	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:11054	urinary bladder cancer Aliases: bladder cancer tumor of the bladder	ENO1 ENO2 GIS1 HXK1 PBS2 RHO1 SMF3	850614 850721 851670 853169 853313 856294 856579	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2355	anemia Aliases: anaemia	HXK1 HXK2 SMF3 ZWF1	850614 850721 852639 855480	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:4194	glucose metabolism disease Aliases: disorder of glucose metabolism	EMI2 HXK1 HXK2	850614 852128 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2861	congenital nonspherocytic hemolytic anemia Aliases: HNSHA congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia	HXK1 HXK2 PGI1 PYK2 ZWF1	850614 852495 852639 854529 855480	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110196	Charcot-Marie-Tooth disease type 4G Aliases: CMT4G Charcot-Marie-Tooth neuropathy type 4G HMSNR autosomal recessive Charcot-Marie-Tooth disease type 4G hereditary motor and sensory neuropathy Russe type	HXK1 HXK2	850614 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10923	sickle cell anemia Aliases: Hb SC disease Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis Sickle-cell/Hb-C disease without crisis drepanocytosis haemoglobin SC disease hemoglobin SC disease sickle cell anaemia	HXK1 HXK2	850614 852639	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070434	hyperphosphatasia with impaired intellectual development syndrome 2 Aliases: GPIBD6 HPMRS2 glycosylphosphatidylinositol biosynthesis defect 6 hyperphosphatasia with mental retardation syndrome 2	GPI13	850628	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081134	3-methylglutaconic aciduria type 7b	HSP104	850633	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0081133	3-methylglutaconic aciduria type 7a	HSP104	850633	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050590	severe congenital neutropenia	HSP104	850633	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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