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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 11501 - 11525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0111671 primary hyperoxaluria type 2 HGNC:4570 Homo sapiens (human) 9380 GRHPR
  • MGI:6194238
  • RGD:7240710
DOID:0110210 Charcot-Marie-Tooth disease X-linked recessive 5 HGNC:9462 Homo sapiens (human) 5631 PRPS1
  • MGI:6194238
  • RGD:7240710
DOID:0060537 mitochondrial complex II deficiency HGNC:10680 Homo sapiens (human) 6389 SDHA
  • MGI:6194238
  • RGD:7240710
DOID:0111670 primary hyperoxaluria type 1 HGNC:341 Homo sapiens (human) 189 AGXT
  • MGI:6194238
  • RGD:7240710
DOID:0090129 carnitine palmitoyltransferase I deficiency HGNC:2328 Homo sapiens (human) 1374 CPT1A
  • MGI:6194238
  • RGD:7240710
DOID:0060248 Simpson-Golabi-Behmel syndrome type 1 HGNC:4451 Homo sapiens (human) 2719 GPC3
  • MGI:6194238
  • RGD:7240710
DOID:0080552 congenital disorder of glycosylation Ia HGNC:9115 Homo sapiens (human) 5373 PMM2
  • MGI:6194238
  • RGD:7240710
DOID:0080240 non-syndromic X-linked intellectual disability 106 HGNC:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
  • RGD:7240710
DOID:0060900 Parkinson's disease 14 HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
  • RGD:7240710
DOID:0112321 alacrima, achalasia, and impaired intellectual development syndrome HGNC:22923 Homo sapiens (human) 29926 GMPPA
  • MGI:6194238
  • RGD:7240710
DOID:0110914 infantile hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
  • RGD:7240710
DOID:0080433 developmental and epileptic encephalopathy 51 HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
  • RGD:7240710
DOID:0060639 permanent neonatal diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • RGD:7240710
DOID:0110721 neuronal ceroid lipofuscinosis 1 HGNC:9325 Homo sapiens (human) 5538 PPT1
  • MGI:6194238
  • RGD:7240710
DOID:0050816 urofacial syndrome HGNC:18374 Homo sapiens (human) 60495 HPSE2
  • MGI:6194238
  • RGD:7240710
DOID:0080572 congenital disorder of glycosylation Iw HGNC:6172 Homo sapiens (human) 3703 STT3A
  • MGI:6194238
  • RGD:7240710
DOID:0070113 Niemann-Pick disease type C1 HGNC:7897 Homo sapiens (human) 4864 NPC1
  • MGI:6194238
  • RGD:7240710
DOID:0070152 hereditary sensory and autonomic neuropathy type 1A HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • MGI:6194238
  • RGD:7240710
DOID:0080201 Peters plus syndrome HGNC:20207 Homo sapiens (human) 145173 B3GLCT
  • MGI:6194238
  • RGD:7240710
DOID:0070263 congenital disorder of glycosylation type IIk HGNC:30760 Homo sapiens (human) 55858 TMEM165
  • MGI:6194238
  • RGD:7240710
DOID:0111100 maturity-onset diabetes of the young type 2 HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • RGD:7240710
DOID:0080101 Compton-North congenital myopathy HGNC:2171 Homo sapiens (human) 1272 CNTN1
  • MGI:6194238
  • RGD:7240710
DOID:0090032 Silverman-Handmaker type dyssegmental dysplasia HGNC:5273 Homo sapiens (human) 3339 HSPG2
  • MGI:6194238
  • RGD:7240710
DOID:14501 Sjogren-Larsson syndrome HGNC:403 Homo sapiens (human) 224 ALDH3A2
  • MGI:6194238
  • RGD:7240710
DOID:0111135 congenital generalized lipodystrophy type 1 HGNC:325 Homo sapiens (human) 10555 AGPAT2
  • MGI:6194238
  • RGD:7240710

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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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