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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 October 9, 2024
Displaying entries 65151 - 65175 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2526 prostate adenocarcinoma HGNC:11362 Homo sapiens (human) 6772 STAT1
  • PMID:9748134
DOID:3314 angiomyolipoma HGNC:11362 Homo sapiens (human) 6772 STAT1
  • PMID:15994429
DOID:0111944 immunodeficiency 31B HGNC:11362 Homo sapiens (human) 6772 STAT1
  • RGD:7240710
DOID:0111946 immunodeficiency 31C HGNC:11362 Homo sapiens (human) 6772 STAT1
  • RGD:7240710
DOID:3770 pulmonary fibrosis HGNC:11362 Homo sapiens (human) 6772 STAT1
  • MGI:6194238
DOID:3717 gastric adenocarcinoma HGNC:11362 Homo sapiens (human) 6772 STAT1
  • PMID:33042401
DOID:1883 hepatitis C HGNC:11362 Homo sapiens (human) 6772 STAT1
  • PMID:26216956
DOID:2154 nephroblastoma HGNC:11362 Homo sapiens (human) 6772 STAT1
  • PMID:16799645
DOID:3319 lymphangioleiomyomatosis HGNC:11362 Homo sapiens (human) 6772 STAT1
  • PMID:15994429
DOID:2841 asthma HGNC:11362 Homo sapiens (human) 6772 STAT1
  • MGI:6194238
DOID:1612 breast cancer HGNC:11362 Homo sapiens (human) 6772 STAT1
  • MGI:6194238
  • PMID:17868458
DOID:9970 obesity HGNC:11362 Homo sapiens (human) 6772 STAT1
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease HGNC:11362 Homo sapiens (human) 6772 STAT1
  • MGI:6194238
DOID:234 colon adenocarcinoma HGNC:11362 Homo sapiens (human) 6772 STAT1
  • PMID:22121102
DOID:0111945 immunodeficiency 31A HGNC:11362 Homo sapiens (human) 6772 STAT1
  • RGD:7240710
DOID:0080322 polycystic kidney disease HGNC:11358 Homo sapiens (human) 10254 STAM2
  • MGI:6194238
DOID:0080865 primary ovarian insufficiency 8 HGNC:11356 Homo sapiens (human) 10734 STAG3
  • RGD:7240710
DOID:0112350 spermatogenic failure 61 HGNC:11356 Homo sapiens (human) 10734 STAG3
  • RGD:7240710
DOID:0080238 autosomal dominant intellectual developmental disorder 47 HGNC:11354 Homo sapiens (human) 10274 STAG1
  • RGD:7240710
DOID:3388 periodontal disease HGNC:11346 Homo sapiens (human) 11009 IL24
  • MGI:6194238
DOID:2999 granulosa cell tumor HGNC:11344 Homo sapiens (human) 6768 ST14
  • PMID:16439987
DOID:4450 renal cell carcinoma HGNC:11344 Homo sapiens (human) 6768 ST14
  • PMID:16501837
DOID:0060074 ductal carcinoma in situ HGNC:11344 Homo sapiens (human) 6768 ST14
  • PMID:17163404
DOID:0060720 autosomal recessive congenital ichthyosis 11 HGNC:11344 Homo sapiens (human) 6768 ST14
  • RGD:7240710
DOID:8634 prostate carcinoma in situ HGNC:11344 Homo sapiens (human) 6768 ST14
  • PMID:18813126

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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: December 9, 2024