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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 70776 - 70800 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:10763 hypertension HGNC:7166 Homo sapiens (human) 4313 MMP2
  • MGI:6194238
  • PMID:16840178
DOID:684 hepatocellular carcinoma HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • MGI:6194238
  • PMID:16835748
  • PMID:18544126
  • PMID:24445728
  • PMID:26930285
  • PMID:27338800
  • PMID:28147320
DOID:11054 urinary bladder cancer HGNC:9052 Homo sapiens (human) 5328 PLAU
  • MGI:6194238
  • PMID:16825821
  • PMID:18336603
DOID:9352 type 2 diabetes mellitus HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
  • PMID:16822679
  • PMID:18472407
  • PMID:19622782
  • PMID:24655058
  • PMID:28843383
DOID:10283 prostate cancer HGNC:11284 Homo sapiens (human) 6715 SRD5A1
  • MGI:6194238
  • PMID:16818707
  • PMID:17720776
DOID:4947 cholangiocarcinoma HGNC:7029 Homo sapiens (human) 4233 MET
  • MGI:6194238
  • PMID:16818635
DOID:9352 type 2 diabetes mellitus HGNC:9235 Homo sapiens (human) 5467 PPARD
  • MGI:6194238
  • PMID:16804087
DOID:13810 familial hypercholesterolemia HGNC:6547 Homo sapiens (human) 3949 LDLR
  • MGI:6194238
  • PMID:16796766
  • PMID:1867200
  • RGD:7240710
DOID:9970 obesity HGNC:3569 Homo sapiens (human) 2180 ACSL1
  • MGI:6194238
  • PMID:16788709
DOID:1561 cognitive disorder HGNC:2695 Homo sapiens (human) 1627 DBN1
  • MGI:6194238
  • PMID:16783169
DOID:6432 pulmonary hypertension HGNC:5318 Homo sapiens (human) 3371 TNC
  • MGI:6194238
  • PMID:16782755
  • PMID:20528622
DOID:0111037 glycine N-methyltransferase deficiency MGI:1202304 Mus musculus (house mouse) 14711 Gnmt
  • MGI:6194238
  • PMID:16779654
  • PMID:17937387
DOID:4483 rhinitis RGD:3644 Rattus norvegicus (Norway rat) 29397 Ccl11
  • MGI:6194238
  • PMID:16765544
DOID:0050328 congenital hypothyroidism MGI:98813 Mus musculus (house mouse) 22018 Tpo
  • MGI:6194238
  • PMID:16762971
DOID:13359 Ehlers-Danlos syndrome ZFIN:ZDB-GENE-040727-3 Danio rerio (zebrafish) 445022 b4galt7
  • MGI:6194238
  • PMID:16759393
DOID:8398 osteoarthritis HGNC:2200 Homo sapiens (human) 1280 COL2A1
  • MGI:6194238
  • PMID:16755660
DOID:14261 fragile X syndrome HGNC:3775 Homo sapiens (human) 2332 FMR1
  • MGI:6194238
  • PMID:1675488
  • RGD:7240710
DOID:1407 anterior uveitis RGD:2232 Rattus norvegicus (Norway rat) 24232 C3
  • MGI:6194238
  • PMID:16751365
DOID:684 hepatocellular carcinoma HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:16750516
DOID:0050741 alcohol dependence HGNC:7808 Homo sapiens (human) 4803 NGF
  • MGI:6194238
  • PMID:16737466
  • PMID:17434673
DOID:0060599 Nance-Horan syndrome HGNC:7820 Homo sapiens (human) 4810 NHS
  • MGI:6194238
  • PMID:16736028
  • RGD:7240710
DOID:5723 optic atrophy HGNC:8140 Homo sapiens (human) 4976 OPA1
  • MGI:6194238
  • PMID:16735988
DOID:5844 myocardial infarction HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:16728681
DOID:9970 obesity HGNC:7978 Homo sapiens (human) 2908 NR3C1
  • MGI:6194238
  • PMID:16725041
  • PMID:18246526
DOID:9352 type 2 diabetes mellitus HGNC:1477 Homo sapiens (human) 11132 CAPN10
  • MGI:6194238
  • PMID:16721485
  • PMID:18554168
  • PMID:19688040
  • PMID:20406624

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Last updated: December 9, 2024