Seroatlas · Human Serome Atlas

ARAF

Serine/threonine-protein kinase A-Raf

Also known as: ARAF_HUMAN, ARAF1

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

Protein identityUniProt · HPA

UniProt accession
P10398
Gene
ARAF
Ensembl
ENSG00000078061
Chromosome
X
Canonical length
606 aa
Protein class
Enzymes, Human disease related genes, Plasma proteins, Predicted intracellular proteins
Subcellular location
Plasma membrane

OverviewNCBI Gene

Enables protein serine/threonine kinase activity. Involved in negative regulation of apoptotic process; regulation of TOR signaling; and regulation of protein metabolic process. Predicted to be active in cytosol and mitochondrion. Biomarker of high grade glioma. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

606 residues, UniProt reviewed canonical sequence.

>P10398|ARAF
     1  MEPPRGPPAN GAEPSRAVGT VKVYLPNKQR TVVTVRDGMS VYDSLDKALK VRGLNQDCCV
    61  VYRLIKGRKT VTAWDTAIAP LDGEELIVEV LEDVPLTMHN FVRKTFFSLA FCDFCLKFLF
   121  HGFRCQTCGY KFHQHCSSKV PTVCVDMSTN RQQFYHSVQD LSGGSRQHEA PSNRPLNELL
   181  TPQGPSPRTQ HCDPEHFPFP APANAPLQRI RSTSTPNVHM VSTTAPMDSN LIQLTGQSFS
   241  TDAAGSRGGS DGTPRGSPSP ASVSSGRKSP HSKSPAEQRE RKSLADDKKK VKNLGYRDSG
   301  YYWEVPPSEV QLLKRIGTGS FGTVFRGRWH GDVAVKVLKV SQPTAEQAQA FKNEMQVLRK
   361  TRHVNILLFM GFMTRPGFAI ITQWCEGSSL YHHLHVADTR FDMVQLIDVA RQTAQGMDYL
   421  HAKNIIHRDL KSNNIFLHEG LTVKIGDFGL ATVKTRWSGA QPLEQPSGSV LWMAAEVIRM
   481  QDPNPYSFQS DVYAYGVVLY ELMTGSLPYS HIGCRDQIIF MVGRGYLSPD LSKISSNCPK
   541  AMRRLLSDCL KFQREERPLF PQILATIELL QRSLPKIERS ASEPSLHRTQ ADELPACLLS
   601  AARLVP

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against ARAF 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
Intracellular
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.42
Highest tissue expression
128 nTPM

Expression across tissuesHPA

Tissue

  • skeletal muscle: 128 nTPM
  • bone marrow: 97 nTPM
  • tongue: 80 nTPM
  • liver: 61 nTPM
  • pancreas: 56 nTPM
  • heart muscle: 53 nTPM

Single-cell type

  • syncytiotrophoblasts: 64 nCPM
  • cholangiocytes: 51 nCPM
  • extravillous trophoblasts: 49 nCPM
  • hepatocytes: 48 nCPM
  • enterocytes: 48 nCPM
  • epididymal principal cells: 48 nCPM

Immune cell

  • non-classical monocyte: 68 nTPM
  • eosinophil: 62 nTPM
  • intermediate monocyte: 58 nTPM
  • myeloid DC: 55 nTPM
  • total PBMC: 51 nTPM
  • basophil: 49 nTPM

Brain region

  • medulla oblongata: 35 nTPM
  • choroid plexus: 34 nTPM
  • thalamus: 32 nTPM
  • basal ganglia: 29 nTPM
  • midbrain: 29 nTPM
  • white matter: 28 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)
0.33
gnomAD pLI
0.96
gnomAD missense Z
2.45
DepMap mean gene effect
0.2
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

InteractionsUniProt · HPA

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

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

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