FRMD8
FERM domain-containing protein 8
Also known as: FKSG44, FLJ90369, FRMD8_HUMAN, iTAP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BZ67
- Gene
- FRMD8
- Ensembl
- ENSG00000126391
- Chromosome
- 11
- Canonical length
- 464 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Centriolar satellite,Cytosol
OverviewNCBI Gene
Involved in positive regulation of tumor necrosis factor production. Located in several cellular components, including centriolar satellite; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
464 residues, UniProt reviewed canonical sequence.
>Q9BZ67|FRMD8
1 MDGTEGSAGQ PGPAERSHRS SVSSVGARAA DVLVYLADDT VVPLAVENLP SLSAHELHRA
61 VREVLQLPDI ALDVFALWLV SPLLEVQLKP KHQPYKLGRQ WPELLLRFTS APDDDVAMDE
121 PFLQFRRNVF FPKRRELQIH DEEVLRLLYE EAKGNVLAAR YPCDVEDCEA LGALVCRVQL
181 GPYQPGRPAA CDLREKLDSF LPAHLCKRGQ SLFAALRGRG ARAGPGEQGL LNAYRQVQEV
241 SSDGGCEAAL GTHYRAYLLK CHELPFYGCA FFHGEVDKPA QGFLHRGGRK PVSVAISLEG
301 VHVIDSREKH VLLGLRFQEL SWDHTSPEEE EPILWLEFDG DSEGTPVNKL LKIYSKQAEL
361 MSSLIEYCIE LSQAAEPAGP QDSATGSPSD PSSSLAPVQR PKLRRQGSVV SSRIQHLSTI
421 DYVEDGKGIR RVKPKRTTSF FSRQLSLGQG SYTVVQPGDS LEQGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FRMD8 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.35
- Highest tissue expression
- 39 nTPM
Expression across tissuesHPA
Tissue
- spleen: 39 nTPM
- esophagus: 36 nTPM
- skin: 33 nTPM
- vagina: 25 nTPM
- small intestine: 23 nTPM
- lung: 23 nTPM
Single-cell type
- esophageal apical cells: 152 nCPM
- urothelial cells: 126 nCPM
- suprabasal keratinocytes: 90 nCPM
- esophageal suprabasal cells: 88 nCPM
- ocular epithelial cells: 80 nCPM
- esophageal basal cells: 64 nCPM
Immune cell
- neutrophil: 23 nTPM
- non-classical monocyte: 20 nTPM
- eosinophil: 18 nTPM
- memory CD8 T-cell: 17 nTPM
- MAIT T-cell: 14 nTPM
- plasmacytoid DC: 13 nTPM
Brain region
- white matter: 33 nTPM
- cerebral cortex: 30 nTPM
- hippocampal formation: 27 nTPM
- medulla oblongata: 27 nTPM
- cerebellum: 25 nTPM
- thalamus: 25 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)
- 0.53
- gnomAD pLI
- 0.11
- gnomAD missense Z
- 0.92
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- selective
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
- negative regulation of canonical Wnt signaling pathway
- positive regulation of tumor necrosis factor production
- protein localization to plasma membrane
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FRMD8 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 FRMD8 as an antibody target. Whether an autoantibody or antibody against FRMD8 could matter depends on whether native FRMD8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FRMD8 is annotated at the cell surface, where native FRMD8 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label FRMD8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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