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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 3251 - 3275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10595 Charcot-Marie-Tooth disease HGNC:16825 Homo sapiens (human) 55613 MTMR8
  • MGI:6194238
DOID:1459 hypothyroidism ZFIN:ZDB-GENE-021031-4 Danio rerio (zebrafish) 556077 plod3
  • MGI:6194238
DOID:684 hepatocellular carcinoma ZFIN:ZDB-GENE-021031-4 Danio rerio (zebrafish) 556077 plod3
  • MGI:6194238
DOID:0060050 autoimmune disease of blood ZFIN:ZDB-GENE-060503-810 Danio rerio (zebrafish) 555344 c1galt1a
  • MGI:6194238
DOID:12140 Chagas disease HGNC:9362 Homo sapiens (human) 5553 PRG2
  • PMID:29545200
DOID:2841 asthma HGNC:9362 Homo sapiens (human) 5553 PRG2
  • PMID:16982448
  • PMID:22022864
  • PMID:24450586
DOID:1725 peritoneum cancer HGNC:9362 Homo sapiens (human) 5553 PRG2
  • PMID:28439450
DOID:0111453 2-aminoadipic 2-oxoadipic aciduria HGNC:23537 Homo sapiens (human) 55526 DHTKD1
  • MGI:6194238
  • RGD:7240710
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q HGNC:23537 Homo sapiens (human) 55526 DHTKD1
  • MGI:6194238
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:0110339 osteogenesis imperfecta type 3 HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:9675 pulmonary emphysema HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • PMID:20448054
DOID:12347 osteogenesis imperfecta HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:0110341 osteogenesis imperfecta type 2 HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:9406 hypopituitarism HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:14240 Homo sapiens (human) 55512 SMPD3
  • MGI:6194238
DOID:10763 hypertension HGNC:17423 Homo sapiens (human) 55501 CHST12
  • MGI:6194238
DOID:10907 microcephaly HGNC:24649 Homo sapiens (human) 55500 ETNK1
  • MGI:6194238
DOID:10273 heart conduction disease HGNC:24649 Homo sapiens (human) 55500 ETNK1
  • MGI:6194238
DOID:1826 epilepsy HGNC:24649 Homo sapiens (human) 55500 ETNK1
  • MGI:6194238
DOID:10763 hypertension ZFIN:ZDB-GENE-030131-9885 Danio rerio (zebrafish) 553944 ugcg
  • MGI:6194238
DOID:14503 neuronal ceroid lipofuscinosis HGNC:9325 Homo sapiens (human) 5538 PPT1
  • MGI:6194238
DOID:0110721 neuronal ceroid lipofuscinosis 1 HGNC:9325 Homo sapiens (human) 5538 PPT1
  • MGI:6194238
  • RGD:7240710
DOID:0110731 neuronal ceroid lipofuscinosis 3 HGNC:9325 Homo sapiens (human) 5538 PPT1
  • MGI:6194238

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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