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 **15101 - 15125** of **15957** in total

« First

‹ Prev

…

601

602

603

604

605

606

607

608

609

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:1172	hyperlipoproteinemia type IV Aliases: Endogenous hyperlipidaemia Fredrickson type IV Lipidemia Fredrickson type IV hyperlipoproteinemia Fredrickson type IV lipidaemia VLDL hyperlipoproteinemia familial hypertriglyceridemia	APOA5 APOC2	116519 344	Homo sapiens (human)	Alliance of Genome Resources
DOID:705	Leber hereditary optic neuropathy Aliases: Leber's hereditary optic neuropathy Leber's optic atrophy	APOA4 ND3 ND5 SOD2 TP53	337 4537 4540 6648 7157	Homo sapiens (human)	Alliance of Genome Resources
DOID:1389	polyneuropathy	APOA4 FCGR3A HLA-DRB1 IL6 SERPINE1 SOD2 SOD3	2214 3123 337 3569 5054 6648 6649	Homo sapiens (human)	Alliance of Genome Resources
DOID:12842	Guillain-Barre syndrome Aliases: Infectious neuronitis Post-infectious polyneuritis Postinfectious polyneuritis acute infective polyneuritis acute inflammatory demyelinating polyradiculopathy acute postinfectious polyneuropathy	APOA4 CCL2 CD86 CTSB GDNF PMP22	1508 2668 337 5376 6347 942	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080958	primary hypoalphalipoproteinemia 2 Aliases: Apolipoprotein A-I deficiency	APOA1	335	Homo sapiens (human)	Alliance of Genome Resources
DOID:11512	Budd-Chiari syndrome Aliases: hepatic vein thrombosis	APOA1 F5	2153 335	Homo sapiens (human)	Alliance of Genome Resources
DOID:687	hepatoblastoma	APOA1 CDH1 CLDN1 CTNNB1 DPEP1 FAS GPC3 MKI67 SALL1 SALL4 SMO SPOP ZFHX3	1499 1800 2719 335 355 4288 463 57167 6299 6608 8405 9076 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080348	Alzheimer's disease 1 Aliases: Alzheimer's disease 1, early onset	APLP1 APLP2 APP KLC2 KLC4 MPO PLAU	333 334 351 4353 5328 64837 89953	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080448	developmental and epileptic encephalopathy 48 Aliases: DEE48 early infantile epileptic encephalopathy 48	APL6	853177	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3082	interstitial lung disease Aliases: ILD	APL6	853177	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1227	neutropenia	APL6	853177	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3770	pulmonary fibrosis Aliases: Fibrosis of lung	APL6 CTS2	851977 853177	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060539	Hermansky-Pudlak syndrome 1	APL5	855906	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2223	platelet storage pool deficiency Aliases: Dense body defect Platelet dense granule deficiency Platelet storage pool defect	APL5 APL6	853177 855906	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:3753	Hermansky-Pudlak syndrome	APL5 APL6	853177 855906	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060540	Hermansky-Pudlak syndrome 2	APL5 APL6	853177 855906	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080016	spina bifida	APEX1 GLI1 GLI2 MTHFD1 MTR PTCH1 RNF2 SUZ12	23512 2735 2736 328 4522 4548 5727 6045	Homo sapiens (human)	Alliance of Genome Resources
DOID:2893	cervix carcinoma Aliases: cancer of cervix carcinoma cervix uteri carcinoma of cervix carcinoma of the Cervix Uteri	APEX1 CD9 EFEMP2 ERAP1 FGFR3 MGMT PTGS1 PTK2 SPARC TK1	2261 30008 328 4255 51752 5742 5747 6678 7083 928	Homo sapiens (human)	Alliance of Genome Resources
DOID:4362	cervical cancer Aliases: cervical neoplasm cervix cancer cervix uteri cancer neoplasm of uterine cervix tumor of the Cervix Uteri uterine cervical neoplasm	APEX1 BIRC2 BRCA1 BSG CD55 CDC25A CDH13 ERBB4 HLA-B HLA-DPB1 HLA-DQB1 HNRNPC HRAS HSPA8 IL10 KDM3A KMT2A KMT2E KRAS MAP2K3 MAP2K6 MDC1 MMP13 MMP1 NRAS PGM3 PTK2 PTPN11 PTPN6 SF3B4 SMAD4 SOS1 TAP1 TNF TNFRSF10A XRCC1 ZFHX3	1012 10262 1604 2066 3106 3115 3119 3183 3265 328 329 3312 3586 3845 4089 4297 4312 4322 463 4893 5238 55818 55904 5606 5608 5747 5777 5781 6654 672 682 6890 7124 7515 8797 9656 993	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110698	hypotrichosis 1 Aliases: Hhs Hts Hypt1 hereditary generalized hypotrichosis simplex	APCDD1 SNRPE	147495 6635	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112104	Sotos syndrome 3 Aliases: SOTOS3	APC2	10297	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081218	autosomal recessive intellectual developmental disorder 74	APC2	10297	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090131	complex cortical dysplasia with other brain malformations Aliases: CDCBM	APC2 CAMSAP1 FOXP1 HCN1	10297 157922 27086 348980	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080409	familial adenomatous polyposis 1	APC2 APC	10297 324	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111349	hereditary desmoid disease Aliases: FIF familial infiltrative fibromatosis	APC	324	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