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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 71076 - 71100 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:2841 asthma HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:12640628
DOID:13777 epidermodysplasia verruciformis HGNC:20474 Homo sapiens (human) 147138 TMC8
  • RGD:7240710
DOID:0111305 familial febrile seizures 4 HGNC:17416 Homo sapiens (human) 84059 ADGRV1
  • RGD:7240710
DOID:11563 retinal vasculitis HGNC:4932 Homo sapiens (human) 3106 HLA-B
  • PMID:12608042
DOID:0111463 cardiofaciocutaneous syndrome 4 HGNC:6842 Homo sapiens (human) 5605 MAP2K2
  • PMID:20358587
  • RGD:7240710
DOID:10608 celiac disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:18728522
DOID:2256 osteochondrodysplasia HGNC:9608 Homo sapiens (human) 5745 PTH1R
  • PMID:8703170
DOID:0081236 autosomal recessive intellectual developmental disorder 77 HGNC:24866 Homo sapiens (human) 9731 CEP104
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:17362997
  • PMID:21767974
DOID:2841 asthma HGNC:7512 Homo sapiens (human) 4583 MUC2
  • PMID:11062147
DOID:1380 endometrial cancer HGNC:10839 Homo sapiens (human) 6462 SHBG
  • PMID:17315164
DOID:7148 rheumatoid arthritis HGNC:11919 Homo sapiens (human) 958 CD40
  • PMID:20498205
DOID:3312 bipolar disorder HGNC:10934 Homo sapiens (human) 6570 SLC18A1
  • PMID:16936705
DOID:0110777 hereditary spastic paraplegia 26 HGNC:4117 Homo sapiens (human) 2583 B4GALNT1
  • RGD:7240710
DOID:10123 pigmentation disease HGNC:6343 Homo sapiens (human) 4254 KITLG
  • RGD:7240710
DOID:1555 urticaria HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:18159608
DOID:0081371 lacrimoauriculodentodigital syndrome 2 HGNC:3690 Homo sapiens (human) 2261 FGFR3
  • RGD:7240710
DOID:5041 esophageal cancer HGNC:12828 Homo sapiens (human) 7515 XRCC1
  • PMID:24345911
DOID:0080376 trichorhinophalangeal syndrome type III HGNC:12340 Homo sapiens (human) 7227 TRPS1
  • RGD:7240710
DOID:670 amphetamine abuse HGNC:7956 Homo sapiens (human) 4886 NPY1R
  • PMID:19566775
DOID:2582 acatalasia HGNC:1516 Homo sapiens (human) 847 CAT
  • RGD:7240710
DOID:0060669 cerebral cavernous malformation HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • RGD:7240710
DOID:9669 senile cataract HGNC:795 Homo sapiens (human) 472 ATM
  • PMID:29156695
DOID:219 colon cancer HGNC:9236 Homo sapiens (human) 5468 PPARG
  • PMID:10394368
DOID:12306 vitiligo HGNC:2505 Homo sapiens (human) 1493 CTLA4
  • PMID:15649153
  • PMID:18200060
  • PMID:19129082
  • PMID:21794098

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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