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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 12201 - 12225 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:18359 Homo sapiens (human) 145264 SERPINA12
  • MGI:6194238
DOID:0110371 retinitis pigmentosa 56 HGNC:18362 Homo sapiens (human) 50939 IMPG2
  • MGI:6194238
  • RGD:7240710
DOID:0050661 vitelliform macular dystrophy HGNC:18362 Homo sapiens (human) 50939 IMPG2
  • MGI:6194238
  • RGD:7240710
DOID:8970 subacute sclerosing panencephalitis HGNC:18363 Homo sapiens (human) 282618 IFNL1
  • PMID:30077763
DOID:12205 dengue disease HGNC:18363 Homo sapiens (human) 282618 IFNL1
  • PMID:28238051
DOID:2841 asthma HGNC:18363 Homo sapiens (human) 282618 IFNL1
  • PMID:22135341
  • PMID:25784275
DOID:1883 hepatitis C HGNC:18363 Homo sapiens (human) 282618 IFNL1
  • PMID:24269996
DOID:684 hepatocellular carcinoma HGNC:18363 Homo sapiens (human) 282618 IFNL1
  • PMID:24769671
DOID:0080600 COVID-19 HGNC:18363 Homo sapiens (human) 282618 IFNL1
  • PMID:32854108
DOID:12206 dengue hemorrhagic fever HGNC:18363 Homo sapiens (human) 282618 IFNL1
  • PMID:31981768
DOID:321 tropical spastic paraparesis HGNC:18363 Homo sapiens (human) 282618 IFNL1
  • PMID:29990995
DOID:0050816 urofacial syndrome HGNC:18374 Homo sapiens (human) 60495 HPSE2
  • MGI:6194238
  • RGD:7240710
DOID:13096 Sneddon syndrome HGNC:1839 Homo sapiens (human) 51816 ADA2
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:1839 Homo sapiens (human) 51816 ADA2
  • PMID:19460251
DOID:106 pleural tuberculosis HGNC:1839 Homo sapiens (human) 51816 ADA2
  • PMID:8656037
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:18410 Homo sapiens (human) 23036 ZNF292
  • RGD:7240710
DOID:12858 Huntington's disease HGNC:18413 Homo sapiens (human) 54503 ZDHHC13
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:18420 Homo sapiens (human) 29072 SETD2
  • PMID:24925220
  • PMID:26069251
DOID:0050156 idiopathic pulmonary fibrosis HGNC:18420 Homo sapiens (human) 29072 SETD2
  • PMID:33533494
DOID:1790 malignant mesothelioma HGNC:18420 Homo sapiens (human) 29072 SETD2
  • PMID:27834213
DOID:9253 gastrointestinal stromal tumor HGNC:18420 Homo sapiens (human) 29072 SETD2
  • PMID:26338826
DOID:10534 stomach cancer HGNC:18420 Homo sapiens (human) 29072 SETD2
  • PMID:29522714
DOID:162 cancer HGNC:18420 Homo sapiens (human) 29072 SETD2
  • MGI:6194238
DOID:7474 malignant pleural mesothelioma HGNC:18420 Homo sapiens (human) 29072 SETD2
  • PMID:26928227
  • PMID:33691361
DOID:0060307 autosomal dominant intellectual developmental disorder HGNC:18420 Homo sapiens (human) 29072 SETD2
  • 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