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 **1351 - 1375** of **4649** in total

« First

‹ Prev

…

51

52

53

54

55

56

57

58

59

…

Next ›

Last »
Disease ID ▲	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0080586	Van Maldergem syndrome 2	FAT4	79633	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080588	agammaglobulinemia 5	LRRC8A	56262	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080589	Klippel-Feil syndrome 1	GDF6	392255	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080591	Klippel-Feil syndrome 3	GDF3	9573	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080592	Klippel-Feil syndrome 4	MYO18B	84700	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080594	hyper IgE recurrent infection syndrome 2	DOCK8	81704	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080596	hyper IgE recurrent infection syndrome 4	IL6ST	3572	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080597	Kleefstra syndrome	EHMT1	79813	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080598	Kleefstra syndrome 2	KMT2C KMT2D	58508 8085	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080599	Coronavirus infectious disease	ACE CCR1 CCR2 CCR5 CD209 EGFR MBL2 MUC4 MYD88 SERPINE1 SFTPD	1230 1234 1636 1956 30835 4153 4585 4615 5054 6441 729230	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080600	COVID-19 Aliases: 2019 Novel Coronavirus (2019-nCoV) 2019-nCoV infection COVID19 SARS-CoV-2 infection Wuhan coronavirus infection Wuhan seafood market pneumonia virus infection	A2M ABO ACE2 ACE AGTR1 ALB ANGPT2 BDH1 BTK C3 C4BPA C4BPB CALCA CCL2 CCL5 CCL7 CD4 CD8A CFH CSF1 CSF2 CSF3 CXCL16 ELANE F2 F3 FTH1 GFAP GZMB HGF HLA-B HLA-C IFNB1 IFNG IFNL1 IL10 IL13 IL17A IL1R1 IL2 IL2RA IL2RB IL2RG IL4 IL6 IL7 IL9 KIR3DS1 LCN2 LGALS3 MMP1 MMP2 MMP8 NEFL NPPB NRP1 PDGFB PLG SELE SERPINF2 SERPING1 THBS1 TLR7 TNF VEGFA	1435 1437 1440 1636 185 1991 2 213 2147 2152 2495 2670 28 282618 285 3002 3075 3082 3106 3107 3456 3458 3554 3558 3559 3560 3561 3565 3569 3574 3578 3586 3596 3605 3813 3934 3958 4312 4313 4317 4747 4879 51284 5155 5340 5345 58191 59272 622 6347 6352 6354 6401 695 7057 710 7124 718 722 725 7422 796 8829 920 925	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080608	anterior segment dysgenesis 3	FOXC1	2296	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080609	anterior segment dysgenesis 4	PITX2	5308	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080611	anterior segment dysgenesis 6	CYP1B1	1545	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080612	anterior segment dysgenesis 7	PXDN	7837	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080615	nephroma Aliases: benign nephroma	DICER1	23405	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080620	familial glucocorticoid deficiency	NNT	23530	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080621	glucocorticoid deficiency 1	MC2R	4158	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080625	severe congenital neutropenia 1	ELANE	1991	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080626	corticosterone methyloxidase deficiency 1 Aliases: aldosterone synthase deficiency	CYP11B2	1585	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080628	alopecia-mental retardation syndrome 1	AHSG	197	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080630	B-lymphoblastic leukemia/lymphoma Aliases: B lymphoblastic leukemia/lymphoma B-ALL precursor B lymphoblastic lymphoma/leukemia	ABL1 AKR1C3 BRD2 CYP3A5 F13A1 F3 FLT3 IKZF1 STAT5A TFPI TNFSF13 TP53	10320 1577 2152 2162 2322 25 6046 6776 7035 7157 8644 8741	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080631	Elsahy-Waters syndrome Aliases: branchioskeletogenital syndrome	CDH11	1009	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080632	Fazio-Londe disease Aliases: riboflavin transporter deficiency neuronopathy	SLC52A3	113278	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080633	developmental cardiac valvular defect	MTHFD1 PLD1 PLD2	4522 5337 5338	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