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 **301 - 325** of **4649** in total

« First

‹ Prev

…

9

10

11

12

13

14

15

16

17

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:0050965	spinocerebellar ataxia type 15 Aliases: spinocerebellar ataxia type 16	ITPR1	3708	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050967	spinocerebellar ataxia type 17	TBP	6908	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050968	autosomal dominant cerebellar ataxia, deafness and narcolepsy	DNMT1	1786	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050974	spinocerebellar ataxia type 25	PNPT1	87178	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050975	spinocerebellar ataxia type 26	EEF2	1938	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050978	spinocerebellar ataxia type 29	ITPR1	3708	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050981	spinocerebellar ataxia type 34	ELOVL4	6785	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050983	spinocerebellar ataxia type 36	NOP56	10528	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050984	spinocerebellar ataxia type 37	DAB1	1600	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050985	spinocerebellar ataxia type 38	ELOVL5	60481	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050986	spinocerebellar ataxia type 40	CCDC88C	440193	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050987	hypomyelinating leukoencephalopathy	KARS1 VPS11	3735 55823	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050989	episodic ataxia type 1	KCNA10 KCNA1 KCNA2 KCNA3 KCNA4 KCNA7	3736 3737 3738 3739 3743 3744	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050990	episodic ataxia type 2	CACNA1A	773	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050994	episodic ataxia type 6	SLC1A1 SLC1A3 SLC1A4 SLC1A5 SLC1A6 SLC1A7	6505 6507 6509 6510 6511 6512	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome Aliases: CAMRQ Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 (CAMRQ1) Uner Tan syndrome VLDLR Cerebellar Hypoplasia	TUBB1 TUBB2A TUBB2B TUBB3 TUBB4A TUBB4B TUBB6 TUBB	10381 10382 10383 203068 347733 7280 81027 84617	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050998	nonprogressive cerebellar ataxia with mental retardation	CAMTA1	23261	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060000	infective endocarditis	TLR6	10333	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060001	withdrawal disorder	AGO2 BDNF CAMK4 COMT CREB1 DRD1 FMR1 FOSB GAD1 GAD2 GRIA1 GRIN2A GRIN2B HTR1A HTR2A HTR2C KCNMA1 KCNU1 KDM4C NGF OPRD1 OPRK1 OPRM1 PRL PTGER3 SLC6A1	1312 1385 157855 1812 23081 2332 2354 2571 2572 27161 2890 2903 2904 3350 3356 3358 3778 4803 4985 4986 4988 5617 5733 627 6529 814	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060009	MHC class I deficiency Aliases: BLS, TYPE I BLSI HLA CLASS I DEFICIENCY bare lymphocyte syndrome type I	TAP1	6890	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060010	Omenn syndrome Aliases: combined immunodeficiency with hypereosinophilia	DCLRE1C	64421	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060013	X-linked severe combined immunodeficiency Aliases: SCID-X1 XSCID gamma chain deficiency thymic epithelial hypoplasia	IL2RG	3561	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060019	coronin-1A deficiency	CORO1A	11151	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060020	reticular dysgenesis Aliases: De Vaal disease	AK2	204	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060022	CD40 ligand deficiency Aliases: HIGMX-1 X-linked hyper-IgM syndrome	CD40LG	959	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