GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

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

Displaying entries **13276 - 13300** of **15957** in total

« First

‹ Prev

…

528

529

530

531

532

533

534

535

536

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:9452	steatotic liver disease Aliases: Fatty change of liver SLD Steatosis of liver alcoholic fatty liver fatty liver disease hepatic lipidosis hepatic steatosis	BPT1 DGA1 ECM38 EMI2 GLK1 HFA1 HXK1 HXK2 KAR2 LAG1 PHO8 POX1	850317 850614 850645 851006 852092 852128 852639 852667 853418 854419 855247 856386	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	BPT1 BUD2 CTS2 EMI2 GLK1 GLR1 HMG1 HMG2 HXK1 HXK2 OGG1 VVS1	850317 850614 850645 851171 851977 852128 852543 852639 853770 854900 854942 856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0112224	chondrodysplasia with joint dislocations gPAPP type Aliases: gPAPP deficiency	BPNT2	54928	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111630	familial erythrocytosis 8 Aliases: BPGM deficiency DPGM deficiency ECYT8 bisphosphoglycerate mutase deficiency bisphosphoglyceromutase deficiency diphosphoglycerate mutase deficiency of erythrocyte hemolytic anemia due to diphosphoglycerate mutase deficiency	BPGM	669	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080858	primary ovarian insufficiency 2A	BNI1	855450	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5426	primary ovarian insufficiency Aliases: hypergonadotropic hypogonadism premature ovarian failure premature ovarian insufficiency	BNI1	855450	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060690	autosomal dominant auditory neuropathy 1 Aliases: AUNA1 NSDAN nonsyndromic dominant auditory neuropathy	BNI1	855450	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110541	autosomal dominant nonsyndromic deafness 1 Aliases: DFNA1 Konigsmark syndrome LFHL1 autosomal dominant deafness 1 autosomal dominant deafness 1, with or without thrombocytopenia hereditary low frequency hearing loss 1	BNI1	855450	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10003	sensorineural hearing loss Aliases: High Frequency Hearing Loss High frequency deafness Perceptive deafness Perceptive hearing loss Perceptive hearing loss or deafness Sensorineural Deafness Sensory hearing loss central hearing loss high-frequency hearing loss	BNI1 MMP1 PUT4 SAM3	850665 854530 855450 855854	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080661	nonsyndromic aplasia cutis congenita	BMS1	9790	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081268	pulmonary venoocclusive disease 1	BMPR2	659	Homo sapiens (human)	Alliance of Genome Resources
DOID:1681	heart septal defect Aliases: Cardiac septal defects Congenital septal defect of heart septal defect	BMPR2 CRELD1 TBX2	659 6909 78987	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110978	brachydactyly type A1D Aliases: BDA1D	BMPR1B	658	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081237	acromesomelic dysplasia-3 Aliases: Demirhan-type acromesomelic dysplasia	BMPR1B	658	Homo sapiens (human)	Alliance of Genome Resources
DOID:14289	Ebstein anomaly Aliases: Ebstein's anomaly Ebstein's anomaly of common atrioventricular valve Ebstein's anomaly of right atrioventricular valve Ebstein's anomaly of tricuspid valve	BMPR1A	657	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060389	chromosome 10q23 deletion syndrome	BMPR1A	657	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111686	hereditary mixed polyposis syndrome 2 Aliases: HMPS2	BMPR1A	657	Homo sapiens (human)	Alliance of Genome Resources
DOID:384	Wolff-Parkinson-White syndrome Aliases: Anomalous A-V excitation Wolff-Parkinson-White pattern anomalous atrioventricular excitation	BMPR1A MAP3K7 PRKAG2 PRKAG3	51422 53632 657 6885	Homo sapiens (human)	Alliance of Genome Resources
DOID:12556	acute kidney tubular necrosis Aliases: ATN - acute tubular necrosis acute renal Failure with tubular necrosis acute renal failure with lesion of tubular necrosis acute tubular necrosis acute tubule necrosis	BMP7 HAVCR1 NOG TEK	26762 655 7010 9241	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060306	Meier-Gorlin syndrome Aliases: ear-patella-short stature syndrome	BMP5	653	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111805	syndromic microphthalmia 6 Aliases: Bakrania-Ragge syndrome MCOPS6 anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia microphthalmia and pituitary anomalies microphthalmia with brain and digit anomalies syndromic microphthalmia type 6	BMP4	652	Homo sapiens (human)	Alliance of Genome Resources
DOID:540	strabismus	BMP4	652	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080015	physical disorder Aliases: congenital disorder	BMP4	652	Homo sapiens (human)	Alliance of Genome Resources
DOID:668	myositis ossificans Aliases: Myisitis ossificans Ossification - muscle	BMP4	652	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080313	cleft palate-lateral synechia syndrome Aliases: CPLS syndrome syngnathia	BMP4	652	Homo sapiens (human)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements