Seroatlas · Human Serome Atlas

HACD4

Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4

Also known as: Em:AL662879.1, HACD4_HUMAN, PTPLAD2

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q5VWC8
Gene
HACD4
Ensembl
ENSG00000188921
Chromosome
9
Canonical length
232 aa
Protein class
Enzymes, Metabolic proteins, Predicted membrane proteins

OverviewNCBI Gene

Enables enzyme binding activity and very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase activity. Involved in fatty acid elongation and very long-chain fatty acid biosynthetic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

232 residues, UniProt reviewed canonical sequence.

>Q5VWC8|HACD4
     1  MGPLALPAWL QPRYRKNAYL FIYYLIQFCG HSWIFTNMTV RFFSFGKDSM VDTFYAIGLV
    61  MRLCQSVSLL ELLHIYVGIE SNHLLPRFLQ LTERIIILFV VITSQEEVQE KYVVCVLFVF
   121  WNLLDMVRYT YSMLSVIGIS YAVLTWLSQT LWMPIYPLCV LAEAFAIYQS LPYFESFGTY
   181  STKLPFDLSI YFPYVLKIYL MMLFIGMYFT YSHLYSERRD ILGIFPIKKK KM

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against HACD4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.

Antibody reachability
Other membrane
Secreted
No
Transmembrane segments
6
Mean surface accessibility (rSASA)
0.31
Highest tissue expression
11 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 11 nTPM
  • lung: 7.8 nTPM
  • placenta: 6 nTPM
  • cervix: 4.9 nTPM
  • thymus: 4.8 nTPM
  • ovary: 4.3 nTPM

Single-cell type

  • platelets: 500 nCPM
  • megakaryocytes: 173 nCPM
  • neutrophils: 139 nCPM
  • respiratory ciliated cells: 107 nCPM
  • neutrophil progenitors: 104 nCPM
  • hofbauer cells: 101 nCPM

Immune cell

  • basophil: 21 nTPM
  • eosinophil: 14 nTPM
  • neutrophil: 12 nTPM
  • non-classical monocyte: 11 nTPM
  • intermediate monocyte: 11 nTPM
  • myeloid DC: 10 nTPM

Brain region

  • choroid plexus: 9.5 nTPM
  • cerebral cortex: 8.7 nTPM
  • cerebellum: 7.6 nTPM
  • white matter: 6.7 nTPM
  • amygdala: 6.3 nTPM
  • basal ganglia: 6.3 nTPM

Genetic constraint and essentialitygnomAD · DepMap

Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.

gnomAD LOEUF (loss-of-function intolerance)
1.19
gnomAD pLI
0
DepMap mean gene effect
0.21
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads HACD4 as an antibody target. Whether an autoantibody or antibody against HACD4 could matter depends on whether native HACD4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

HACD4 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.

Annotation status

The present source text does not explicitly label HACD4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/HACD4. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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