mannosidase alpha class 2C member 1

Summary
Gene Symbol
  • MAN2C1
Organism
Homo sapiens (human)
External Links
NCBI Gene
4123
HGNC
6827
KEGG Gene ID
hsa:4123
PubChem
4123
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cobalt
  • Cytoplasm
  • Glycosidase
  • Metal-binding
  • Reference proteome
Proteins
Displaying all 2 entries
UniProt Protein Name
Q9NTJ4
  • Alpha mannosidase 6A8B
  • Alpha-D-mannoside mannohydrolase
  • Mannosidase alpha class 2C member 1
A0A140VJN9
Gene Ontology (GO)
Displaying all 2 entries
GO Term Evidence Code PMID
cytosol
nucleoplasm
KEGG BRITE Database
Orthology
K01191
Name
alpha-mannosidase [EC:3.2.1.24]
References
Disease
Disease Ontology
Displaying entries 11 - 12 of 12 in total
DO ID Disease Name Source
DOID:5041 esophageal cancer
DOID:8927 learning disability
The Human Phenotype Ontology
Displaying entries 11 - 20 of 33 in total
HPO ID HPO Term
HP:0000750 Delayed speech and language development
HP:0000960 Sacral dimple
HP:0001249 Intellectual disability
HP:0001252 Hypotonia
HP:0001270 Motor delay
HP:0001320 Cerebellar vermis hypoplasia
HP:0001338 Partial agenesis of the corpus callosum
HP:0001776 Bilateral talipes equinovarus
HP:0001852 Sandal gap
HP:0002000 Short columella
Displaying 1 entry
Disease ID Disease Name
OMIM:619775
  • congenital disorder of deglycosylation 2

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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