3-hydroxyacyl-CoA dehydratase 1

Summary
Gene Symbol
  • HACD1
Aliases
  • CAP
  • Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1
  • cementum attachment protein
Organism
Homo sapiens (human)
NCBI Gene
9200
HGNC
9639
KEGG Gene ID
hsa:9200
PubChem
9200
Alliance of Genome Resources
JoGo
HACD1
TogoVar
HACD1
Annotation
Keyword
  • Alternative splicing
  • Developmental protein
  • Disease variant
  • Endoplasmic reticulum
  • Fatty acid biosynthesis
  • Glycoprotein
  • Lyase
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
B0YJ81
  • 3-hydroxyacyl-CoA dehydratase 1
  • Cementum-attachment protein
  • Protein-tyrosine phosphatase-like member A
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase
Functional Category
  • K: Transcription
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
KEGG BRITE Database
Orthology
K10703
Name
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase [EC:4.2.1.134]
References
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0081337 congenital myopathy
The Human Phenotype Ontology
Displaying entries 61 - 70 of 70 in total
HPO ID HPO Term
HP:0011470 Nasogastric tube feeding in infancy
HP:0011807 Type 1 muscle fiber atrophy
HP:0011842 Abnormal skeletal morphology
HP:0011922 Abnormal activity of mitochondrial respiratory chain
HP:0011951 Aspiration pneumonia
HP:0011968 Feeding difficulties
HP:0012378 Fatigue
HP:0012416 Hypercapnia
HP:0012418 Hypoxemia
HP:0012785 Flexion contracture of finger
Displaying all 2 entries
Disease ID Disease Name
OMIM:619967
  • congenital myopathy 11
ORPHA:2020
  • congenital fiber-type disproportion myopathy

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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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