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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Displaying entries 3551 - 3575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:10762 portal hypertension HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:3492 mixed connective tissue disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19684145
DOID:12662 paracoccidioidomycosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:17145373
DOID:0080162 lupus nephritis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:7750940
DOID:3083 chronic obstructive pulmonary disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:11179116
  • PMID:12537602
  • PMID:15820084
  • PMID:20299531
  • PMID:20352242
  • PMID:20500811
  • PMID:8564092
DOID:841 extrinsic allergic alveolitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15653992
DOID:0050565 autosomal recessive nonsyndromic deafness HGNC:25904 Homo sapiens (human) 84899 TMTC4
  • RGD:7240710
DOID:1826 epilepsy HGNC:26899 Homo sapiens (human) 160418 TMTC3
  • MGI:6194238
DOID:0112233 lissencephaly 8 HGNC:26899 Homo sapiens (human) 160418 TMTC3
  • RGD:7240710
DOID:0081312 T-cell non-Hodgkin lymphoma HGNC:20185 Homo sapiens (human) 54916 TMEM260
  • PMID:24831772
DOID:10534 stomach cancer HGNC:20185 Homo sapiens (human) 54916 TMEM260
  • PMID:27602096
DOID:0060060 non-Hodgkin lymphoma HGNC:20185 Homo sapiens (human) 54916 TMEM260
  • PMID:24831772
DOID:0070268 congenital disorder of glycosylation type IIp HGNC:18085 Homo sapiens (human) 147007 TMEM199
  • RGD:7240710
DOID:0070263 congenital disorder of glycosylation type IIk HGNC:30760 Homo sapiens (human) 55858 TMEM165
  • MGI:6194238
  • RGD:7240710
DOID:0050571 congenital disorder of glycosylation type II HGNC:30760 Homo sapiens (human) 55858 TMEM165
  • MGI:6194238
DOID:2841 asthma HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:15266299
  • PMID:18547625
DOID:8677 perinatal necrotizing enterocolitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • MGI:6194238
DOID:4483 rhinitis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:20815312
DOID:399 tuberculosis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:18091991
DOID:13564 aspergillosis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:16461792
DOID:0060000 infective endocarditis HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:25213166
DOID:874 bacterial pneumonia HGNC:16711 Homo sapiens (human) 10333 TLR6
  • MGI:6194238
DOID:3021 acute kidney failure HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:4989 pancreatitis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:2841 asthma HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:15356557
  • PMID:16266379
  • PMID:19067129
  • PMID:19159017
  • PMID:20685742

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024