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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 63851 - 63875 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus HGNC:1508 Homo sapiens (human) 840 CASP7
  • MGI:6194238
DOID:0060074 ductal carcinoma in situ HGNC:1507 Homo sapiens (human) 839 CASP6
  • PMID:10574243
DOID:1824 status epilepticus HGNC:1507 Homo sapiens (human) 839 CASP6
  • MGI:6194238
DOID:2316 brain ischemia HGNC:1507 Homo sapiens (human) 839 CASP6
  • MGI:6194238
DOID:11132 prostatic hypertrophy HGNC:1507 Homo sapiens (human) 839 CASP6
  • PMID:15507514
DOID:1002 endometritis HGNC:1507 Homo sapiens (human) 839 CASP6
  • MGI:6194238
DOID:4001 ovarian carcinoma HGNC:1507 Homo sapiens (human) 839 CASP6
  • PMID:17283169
DOID:3525 middle cerebral artery infarction HGNC:1507 Homo sapiens (human) 839 CASP6
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:1507 Homo sapiens (human) 839 CASP6
  • PMID:12633148
DOID:8552 chronic myeloid leukemia HGNC:1507 Homo sapiens (human) 839 CASP6
  • PMID:31952546
DOID:3908 lung non-small cell carcinoma HGNC:1507 Homo sapiens (human) 839 CASP6
  • PMID:16231180
DOID:10286 prostate carcinoma HGNC:1507 Homo sapiens (human) 839 CASP6
  • MGI:6194238
DOID:0060309 syndromic X-linked intellectual disability HGNC:1497 Homo sapiens (human) 8573 CASK
  • MGI:6194238
DOID:14711 FG syndrome HGNC:1497 Homo sapiens (human) 8573 CASK
  • PMID:19200522
DOID:0060041 autism spectrum disorder HGNC:1497 Homo sapiens (human) 8573 CASK
  • MGI:6194238
DOID:0060807 syndromic X-linked intellectual disability Najm type HGNC:1497 Homo sapiens (human) 8573 CASK
  • RGD:7240710
DOID:10907 microcephaly HGNC:1493 Homo sapiens (human) 833 CARS1
  • MGI:6194238
DOID:0111984 immunodeficiency 58 HGNC:27089 Homo sapiens (human) 146206 CARMIL2
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:16391 Homo sapiens (human) 64170 CARD9
  • MGI:6194238
DOID:612 primary immunodeficiency disease HGNC:16391 Homo sapiens (human) 64170 CARD9
  • RGD:7240710
DOID:9212 pityriasis rubra pilaris HGNC:16446 Homo sapiens (human) 79092 CARD14
  • RGD:7240710
DOID:0080475 psoriasis 2 HGNC:16446 Homo sapiens (human) 79092 CARD14
  • MGI:6194238
  • RGD:7240710
DOID:0111957 immunodeficiency 11A HGNC:16393 Homo sapiens (human) 84433 CARD11
  • RGD:7240710
DOID:0050745 diffuse large B-cell lymphoma HGNC:16393 Homo sapiens (human) 84433 CARD11
  • PMID:18323416
DOID:5603 T-cell acute lymphoblastic leukemia HGNC:16393 Homo sapiens (human) 84433 CARD11
  • PMID:25384343

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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