Seroatlas · Human Serome Atlas

FAM118B

Protein FAM118B

Also known as: F118B_HUMAN, FLJ21103

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

Protein identityUniProt · HPA

UniProt accession
Q9BPY3
Gene
FAM118B
Ensembl
ENSG00000197798
Chromosome
11
Canonical length
351 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

Enables identical protein binding activity. Predicted to be located in Cajal body. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

351 residues, UniProt reviewed canonical sequence.

>Q9BPY3|FAM118B
     1  MASTGSQASD IDEIFGFFND GEPPTKKPRK LLPSLKTKKP RELVLVIGTG ISAAVAPQVP
    61  ALKSWKGLIQ ALLDAAIDFD LLEDEESKKF QKCLHEDKNL VHVAHDLIQK LSPRTSNVRS
   121  TFFKDCLYEV FDDLESKMED SGKQLLQSVL HLMENGALVL TTNFDNLLEL YAADQGKQLE
   181  SLDLTDEKKV LEWAQEKRKL SVLHIHGVYT NPSGIVLHPA GYQNVLRNTE VMREIQKLYE
   241  NKSFLFLGCG WTVDDTTFQA LFLEAVKHKS DLEHFMLVRR GDVDEFKKLR ENMLDKGIKV
   301  ISYGDDYADL PEYFKRLTCE ISTRGTSAGM VREGQLNGSS AAHSEIRGCS T

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against FAM118B 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)
0.32
Highest tissue expression
29 nTPM

Expression across tissuesHPA

Tissue

  • choroid plexus: 29 nTPM
  • basal ganglia: 23 nTPM
  • colon: 23 nTPM
  • rectum: 22 nTPM
  • skeletal muscle: 22 nTPM
  • testis: 20 nTPM

Single-cell type

  • pituicytes/fscs: 82 nCPM
  • late primary spermatocytes: 72 nCPM
  • myonuclei: 59 nCPM
  • choroid plexus epithelial cells: 55 nCPM
  • cardiomyocytes: 50 nCPM
  • hofbauer cells: 49 nCPM

Immune cell

  • non-classical monocyte: 60 nTPM
  • intermediate monocyte: 59 nTPM
  • myeloid DC: 48 nTPM
  • classical monocyte: 44 nTPM
  • basophil: 34 nTPM
  • total PBMC: 25 nTPM

Brain region

  • choroid plexus: 24 nTPM
  • basal ganglia: 22 nTPM
  • white matter: 16 nTPM
  • hypothalamus: 15 nTPM
  • spinal cord: 15 nTPM
  • cerebral cortex: 15 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)
0.68
gnomAD pLI
0.02
gnomAD missense Z
0.96
DepMap mean gene effect
0.17
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads FAM118B as an antibody target. Whether an autoantibody or antibody against FAM118B could matter depends on whether native FAM118B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

FAM118B 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 FAM118B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/FAM118B. 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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