Seroatlas · Human Serome Atlas

DHFR2

Dihydrofolate reductase 2, mitochondrial

Also known as: DHFRL1, DHFRP4, DYR2_HUMAN, FLJ16119

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

Protein identityUniProt · HPA

UniProt accession
Q86XF0
Gene
DHFR2
Ensembl
ENSG00000178700
Chromosome
3
Canonical length
187 aa
Protein class
Enzymes, Metabolic proteins, Predicted intracellular proteins
Subcellular location
Mitochondria

OverviewNCBI Gene

Enables dihydrofolate reductase activity and mRNA binding activity. Involved in tetrahydrofolate metabolic process and thymidine biosynthetic process. Located in mitochondrial inner membrane and mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

187 residues, UniProt reviewed canonical sequence.

>Q86XF0|DHFR2
     1  MFLLLNCIVA VSQNMGIGKN GDLPRPPLRN EFRYFQRMTT TSSVEGKQNL VIMGRKTWFS
    61  IPEKNRPLKD RINLVLSREL KEPPQGAHFL ARSLDDALKL TERPELANKV DMIWIVGGSS
   121  VYKEAMNHLG HLKLFVTRIM QDFESDTFFS EIDLEKYKLL PEYPGVLSDV QEGKHIKYKF
   181  EVCEKDD

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against DHFR2 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
0
Mean surface accessibility (rSASA)
0.28
Highest tissue expression
8 nTPM

Expression across tissuesHPA

Tissue

  • ovary: 8 nTPM
  • endometrium: 7.3 nTPM
  • liver: 6.2 nTPM
  • thyroid gland: 6.2 nTPM
  • parathyroid gland: 6.1 nTPM
  • cerebral cortex: 6 nTPM

Single-cell type

  • epicardial cells: 46 nCPM
  • cardiomyocytes: 43 nCPM
  • late primary spermatocytes: 41 nCPM
  • tuft cells: 35 nCPM
  • early spermatids: 28 nCPM
  • epididymal principal cells: 28 nCPM

Immune cell

  • MAIT T-cell: 3.3 nTPM
  • naive CD4 T-cell: 3.3 nTPM
  • T-reg: 3.2 nTPM
  • naive CD8 T-cell: 3 nTPM
  • memory CD8 T-cell: 2.9 nTPM
  • memory CD4 T-cell: 2.4 nTPM

Brain region

  • white matter: 16 nTPM
  • cerebellum: 15 nTPM
  • basal ganglia: 14 nTPM
  • cerebral cortex: 14 nTPM
  • pons: 14 nTPM
  • choroid plexus: 13 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)
1.44
gnomAD pLI
0.22
DepMap mean gene effect
-0.46
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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 DHFR2 as an antibody target. Whether an autoantibody or antibody against DHFR2 could matter depends on whether native DHFR2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

DHFR2 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 DHFR2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/DHFR2. 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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