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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **176 - 200** of **5716** in total

« First

‹ Prev

…

4

5

6

7

8

9

10

11

12

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0111442	optic atrophy 9 Aliases: OPA9	ACO2	50	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050883	infantile cerebellar-retinal degeneration	ACO2	50	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070516	Mitchell syndrome	ACOX1	37028	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070516	Mitchell syndrome	ACOX1	51	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050797	peroxisomal acyl-CoA oxidase deficiency Aliases: Peroxisomal acyl-coenzyme A oxidase	ACOX1	51	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111067	congenital bile acid synthesis defect 6 Aliases: CBAS6	ACOX2	8309	Homo sapiens (human)	Alliance of Genome Resources
DOID:10283	prostate cancer Aliases: NGP - new growth of prostate hereditary prostate cancer malignant tumor of the prostate prostate cancer, familial prostate neoplasm prostatic cancer prostatic neoplasm tumor of the prostate	ACP3 ACSL3 AGAP2 AKT1 AKT2 AKT3 APC AR BMP2 BMP7 BRCA1 BRCA2 CADM1 CD44 CD55 CDC25A CDH13 CDH1 CHD1 CHEK2 CHGA CHUK COMT CXCR4 CYP17A1 CYP1A1 EGFR EIF3H ENO2 EPHB1 ERBB2 ESR1 FAS FGFR4 FLT3 GRB2 HIF1A HLA-DRB1 ICAM1 IGFBP3 IKBKB IL16 JAK1 JUP KLK10 KLK4 MAP3K7 MSR1 MTOR MXI1 MYC NAT2 NBN NFKB1 NOS3 OGG1 PDPK1 PEBP1 PIK3CB PTEN PTGS2 RB1 RNASEL SRC SRD5A1 SRD5A2 SREBF2 STAT3 SULT2A1 TLR2 TMEFF2 TNF TP53 TSG101 VDAC1 VEGFA XIAP XRCC1 ZFHX3	10 10000 1012 1105 1113 11200 1147 116986 1312 1543 1586 1604 1956 2026 2047 2064 207 208 2099 2181 2264 2322 23671 23705 2475 2885 3091 3123 324 331 3383 3486 355 3551 3603 367 3716 3728 4481 4601 4609 463 4683 4790 4846 4968 5037 5170 5291 55 5655 5728 5743 5925 6041 650 655 6714 6715 6716 672 6721 675 6774 6822 6885 7097 7124 7157 7251 7416 7422 7515 7852 8667 960 9622 993 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080953	amelogenesis imperfecta type 1J Aliases: Amelogenesis imperfecta, type IJ	ACP4	93650	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112295	spondylometaphyseal dysplasia	ACP5	54	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070586	spermatogenic failure 87 Aliases: SPGF87	ACR	49	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111263	combined malonic and methylmalonic acidemia Aliases: CMAMMA combined malonic and methylmalonic aciduria	ACSF3	197322	Homo sapiens (human)	Alliance of Genome Resources
DOID:1059	intellectual disability	ACSL4 AGTR2 ARHGEF6 ARID1B CASR CC2D1A CC2D2A CDK13 CDKL5 CHKB DMD DRD4 DYRK1A EIF4A3 GPI HPN IL1RAPL1 IMPA1 KRAS NONO PRSS12 RPGRIP1L RPS6KA3 SARS1 SLC6A8 SMC3 TSC1 WDR62	11141 1120 1756 1815 1859 186 2182 23322 2821 284403 3249 3612 3845 4841 54862 57492 57545 6197 6301 6535 6792 7248 846 8492 8621 9126 9459 9775	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112050	non-syndromic X-linked intellectual disability 63 Aliases: ACSL4-related intellectual disability MRX63 MRX68 X-linked mental retardation 63 X-linked mental retardation 68	ACSL4	2182	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060774	congenital diarrhea	ACSL5 PLVAP WNT2B	51703 7482 83483	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050567	orofacial cleft	ACSS2 LOXHD1 MYH9	125336 4627 55902	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081340	congenital myopathy 2C	ACTA1	58	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110927	nemaline myopathy 3 Aliases: NEM3 congenital myopathy 2A nemaline myopathy 3, autosomal dominant or recessive	ACTA1	58	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081339	congenital myopathy 2B	ACTA1	58	Homo sapiens (human)	Alliance of Genome Resources
DOID:13099	Moyamoya disease Aliases: progressive intracranial arterial occlusion	ACTA2 ANO1 HLA-A RNF213	3105 55107 57674 59	Homo sapiens (human)	Alliance of Genome Resources
DOID:14004	thoracic aortic aneurysm	ACTA2 LOX MFAP5 MMP1 MMP9 MYH11 MYLK PRKG1 THSD4	4015 4312 4318 4629 4638 5592 59 79875 8076	Homo sapiens (human)	Alliance of Genome Resources
DOID:1588	thrombocytopenia	ACTB ANKRD26 CCL2 F7 FCGR2A FLI1 FYB1 GALE GNE IL10 ITGA2 ITGA2B ITGB3 MASTL MBL2 MPL MYH9 PTPRJ SRC THPO TNF	10020 2155 2212 22852 2313 2533 2582 3586 3673 3674 3690 4153 4352 4627 5795 60 6347 6714 7066 7124 84930	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081112	Baraitser-Winter syndrome 1	ACTB	60	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110456	dilated cardiomyopathy 1R Aliases: CMD1R	ACTC1	70	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110317	hypertrophic cardiomyopathy 11 Aliases: CMH11 cardiomyopathy familial hypertrophic 11	ACTC1	70	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110110	atrial heart septal defect 5 Aliases: ASD5 atrial septal defect 5	ACTC1	70	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

Guidelines

International Collaboration

Acknowledgements