Seroatlas · Human Serome Atlas

FUNDC2

FUN14 domain-containing protein 2

Also known as: DC44, FUND2_HUMAN, HCBP6

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

Protein identityUniProt · HPA

UniProt accession
Q9BWH2
Gene
FUNDC2
Ensembl
ENSG00000165775
Chromosome
X
Canonical length
189 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

Enables phosphatidylinositol-3,4,5-trisphosphate binding activity. Involved in intracellular triglyceride homeostasis. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

189 residues, UniProt reviewed canonical sequence.

>Q9BWH2|FUNDC2
     1  METSAPRAGS QVVATTARHS AAYRADPLRV SSRDKLTEMA ASSQGNFEGN FESLDLAEFA
    61  KKQPWWRKLF GQESGPSAEK YSVATQLFIG GVTGWCTGFI FQKVGKLAAT AVGGGFFLLQ
   121  LANHTGYIKV DWQRVEKDMK KAKEQLKIRK SNQIPTEVRS KAEEVVSFVK KNVLVTGGFF
   181  GGFLLGMAS

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against FUNDC2 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
3
Mean surface accessibility (rSASA)
0.51
Highest tissue expression
18 nTPM

Expression across tissuesHPA

Tissue

  • tongue: 18 nTPM
  • skeletal muscle: 17 nTPM
  • heart muscle: 9.7 nTPM
  • pancreas: 7.3 nTPM
  • ovary: 5.7 nTPM
  • choroid plexus: 5.3 nTPM

Single-cell type

  • late spermatids: 2,447 nCPM
  • early spermatids: 345 nCPM
  • pancreatic acinar cells: 281 nCPM
  • parietal cells: 210 nCPM
  • decidual stromal cells: 161 nCPM
  • mast cells: 131 nCPM

Immune cell

  • total PBMC: 3.3 nTPM
  • non-classical monocyte: 2.9 nTPM
  • myeloid DC: 2.7 nTPM
  • naive CD8 T-cell: 2.6 nTPM
  • T-reg: 2.6 nTPM
  • gdT-cell: 2.5 nTPM

Brain region

  • cerebellum: 6 nTPM
  • pons: 5.3 nTPM
  • medulla oblongata: 5.1 nTPM
  • thalamus: 5.1 nTPM
  • choroid plexus: 4.9 nTPM
  • spinal cord: 4.9 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)
1.02
gnomAD pLI
0.06
gnomAD missense Z
0.36
DepMap mean gene effect
0.06
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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

InteractionsUniProt · HPA

Protein binding partners of FUNDC2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads FUNDC2 as an antibody target. Whether an autoantibody or antibody against FUNDC2 could matter depends on whether native FUNDC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

FUNDC2 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 FUNDC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/FUNDC2. 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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