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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 66676 - 66700 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5325 Roberts syndrome HGNC:10702 Homo sapiens (human) 10483 SEC23B
  • MGI:6194238
DOID:5325 Roberts syndrome HGNC:10701 Homo sapiens (human) 10484 SEC23A
  • MGI:6194238
DOID:0111401 congenital dyserythropoietic anemia type II HGNC:10701 Homo sapiens (human) 10484 SEC23A
  • MGI:6194238
DOID:0070307 craniolenticulosutural dysplasia HGNC:10701 Homo sapiens (human) 10484 SEC23A
  • MGI:6194238
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:10700 Homo sapiens (human) 9554 SEC22B
  • MGI:6194238
DOID:1508 candidiasis HGNC:10697 Homo sapiens (human) 6396 SEC13
  • MGI:6194238
DOID:0110965 brachydactyly type A2 HGNC:1069 Homo sapiens (human) 650 BMP2
  • RGD:7240710
DOID:10286 prostate carcinoma HGNC:1069 Homo sapiens (human) 650 BMP2
  • PMID:16519147
DOID:0050591 tooth agenesis HGNC:1069 Homo sapiens (human) 650 BMP2
  • PMID:23079991
DOID:0050787 juvenile polyposis syndrome HGNC:1069 Homo sapiens (human) 650 BMP2
  • MGI:6194238
DOID:10283 prostate cancer HGNC:1069 Homo sapiens (human) 650 BMP2
  • PMID:15042598
  • PMID:17656261
DOID:11476 osteoporosis HGNC:1069 Homo sapiens (human) 650 BMP2
  • PMID:17002564
DOID:10763 hypertension HGNC:1069 Homo sapiens (human) 650 BMP2
  • MGI:6194238
DOID:14323 Marfan syndrome HGNC:1069 Homo sapiens (human) 650 BMP2
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:1069 Homo sapiens (human) 650 BMP2
  • PMID:15334463
DOID:12185 otosclerosis HGNC:1069 Homo sapiens (human) 650 BMP2
  • PMID:18021008
DOID:0111029 hemochromatosis type 1 HGNC:1069 Homo sapiens (human) 650 BMP2
  • RGD:7240710
DOID:0060537 mitochondrial complex II deficiency HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
  • RGD:7240710
DOID:0050773 paraganglioma HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
  • PMID:10657297
  • RGD:7240710
DOID:11984 hypertrophic cardiomyopathy HGNC:10683 Homo sapiens (human) 6392 SDHD
  • MGI:6194238
DOID:0080533 Carney-Stratakis syndrome HGNC:10683 Homo sapiens (human) 6392 SDHD
  • RGD:7240710
DOID:9253 gastrointestinal stromal tumor HGNC:10682 Homo sapiens (human) 6391 SDHC
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:25576295
DOID:0050773 paraganglioma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:11062460
  • RGD:7240710
DOID:0080533 Carney-Stratakis syndrome HGNC:10682 Homo sapiens (human) 6391 SDHC
  • RGD:7240710

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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