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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 64226 - 64250 of 71927 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0070151 hereditary sensory and autonomic neuropathy type 6 HGNC:1090 Homo sapiens (human) 667 DST
  • MGI:6194238
  • RGD:7240710
DOID:0070151 hereditary sensory and autonomic neuropathy type 6 MGI:104627 Mus musculus (house mouse) 13518 Dst
  • MGI:6194238
  • PMID:27693510
DOID:0070150 hereditary sensory and autonomic neuropathy type 2B HGNC:25964 Homo sapiens (human) 54463 RETREG1
  • RGD:7240710
DOID:0070149 hereditary sensory and autonomic neuropathy type 7 RGD:3630 Rattus norvegicus (Norway rat) 29701 Scn11a
  • MGI:6194238
DOID:0070149 hereditary sensory and autonomic neuropathy type 7 FB:FBgn0285944 Drosophila melanogaster (fruit fly) 32619 para
  • MGI:6194238
DOID:0070149 hereditary sensory and autonomic neuropathy type 7 MGI:1345149 Mus musculus (house mouse) 24046 Scn11a
  • MGI:6194238
DOID:0070149 hereditary sensory and autonomic neuropathy type 7 HGNC:10583 Homo sapiens (human) 11280 SCN11A
  • RGD:7240710
DOID:0070146 hereditary sensory neuropathy type 4 MGI:97383 Mus musculus (house mouse) 18211 Ntrk1
  • MGI:6194238
DOID:0070146 hereditary sensory neuropathy type 4 RGD:620144 Rattus norvegicus (Norway rat) 59109 Ntrk1
  • MGI:6194238
DOID:0070146 hereditary sensory neuropathy type 4 HGNC:8031 Homo sapiens (human) 4914 NTRK1
  • RGD:7240710
DOID:0070145 hereditary sensory and autonomic neuropathy type 5 MGI:97321 Mus musculus (house mouse) 18049 Ngf
  • MGI:6194238
DOID:0070145 hereditary sensory and autonomic neuropathy type 5 RGD:1598328 Rattus norvegicus (Norway rat) 310738 Ngf
  • MGI:6194238
DOID:0070145 hereditary sensory and autonomic neuropathy type 5 Xenbase:XB-GENE-6500082 Xenopus laevis (African clawed frog) 108709389 ngf.S
  • MGI:6194238
DOID:0070145 hereditary sensory and autonomic neuropathy type 5 HGNC:7808 Homo sapiens (human) 4803 NGF
  • RGD:7240710
DOID:0070145 hereditary sensory and autonomic neuropathy type 5 ZFIN:ZDB-GENE-000629-2 Danio rerio (zebrafish) 58133 ngfb
  • MGI:6194238
DOID:0070143 autosomal recessive cutis laxa type III MGI:1888908 Mus musculus (house mouse) 56454 Aldh18a1
  • MGI:6194238
DOID:0070143 autosomal recessive cutis laxa type III HGNC:9722 Homo sapiens (human) 5832 ALDH18A1
  • PMID:24913064
  • PMID:26320891
DOID:0070140 autosomal recessive cutis laxa type IIC HGNC:857 Homo sapiens (human) 529 ATP6V1E1
  • RGD:7240710
DOID:0070139 autosomal recessive cutis laxa type IC HGNC:6717 Homo sapiens (human) 8425 LTBP4
  • RGD:7240710
DOID:0070139 autosomal recessive cutis laxa type IC MGI:1321395 Mus musculus (house mouse) 108075 Ltbp4
  • MGI:6194238
DOID:0070138 autosomal recessive cutis laxa type IIIB HGNC:9721 Homo sapiens (human) 5831 PYCR1
  • RGD:7240710
DOID:0070137 autosomal recessive cutis laxa type IIB HGNC:30262 Homo sapiens (human) 29920 PYCR2
  • MGI:6194238
DOID:0070137 autosomal recessive cutis laxa type IIB HGNC:9721 Homo sapiens (human) 5831 PYCR1
  • MGI:6194238
  • RGD:7240710
DOID:0070136 autosomal dominant cutis laxa 2 RGD:2594 Rattus norvegicus (Norway rat) 29158 Fbln5
  • MGI:6194238
DOID:0070136 autosomal dominant cutis laxa 2 MGI:1346091 Mus musculus (house mouse) 23876 Fbln5
  • 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: December 9, 2024