arylsulfatase family member H

Summary
Gene Symbol
  • ARSH
Organism
Homo sapiens (human)
External Links
NCBI Gene
347527
HGNC
32488
KEGG Gene ID
hsa:347527
PubChem
347527
Alliance of Genome Resources
Annotation
Keyword
  • Calcium
  • Hydrolase
  • Metal-binding
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q5FYA8
KEGG BRITE Database
Orthology
K12374
Name
arylsulfatase D/F/H [EC:3.1.6.-]
References
Disease
Disease Ontology
Displaying entries 1 - 10 of 37 in total
DO ID Disease Name Source
DOID:0050441 mucosulfatidosis
DOID:0050819 obsolete Matthew-Wood syndrome
DOID:0050908 myelodysplastic syndrome
DOID:0060257 dyschromatosis symmetrica hereditaria
DOID:0060262 gallbladder disease
DOID:0060292 X-linked chondrodysplasia punctata 1
DOID:0060293 autosomal dominant chondrodysplasia punctata
DOID:0110851 rhizomelic chondrodysplasia punctata type 1
DOID:0110852 rhizomelic chondrodysplasia punctata type 2
DOID:0110853 rhizomelic chondrodysplasia punctata type 3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024