FAM168B
Myelin-associated neurite-outgrowth inhibitor
Also known as: F168B_HUMAN, KIAA0280L, MANI
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A1KXE4
- Gene
- FAM168B
- Ensembl
- ENSG00000152102
- Chromosome
- 2
- Canonical length
- 195 aa
- Protein class
- Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Predicted to act upstream of or within axonogenesis and gene expression. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
195 residues, UniProt reviewed canonical sequence.
>A1KXE4|FAM168B
1 MNPVYSPGSS GVPYANAKGI GYPAGFPMGY AAAAPAYSPN MYPGANPTFQ TGYTPGTPYK
61 VSCSPTSGAV PPYSSSPNPY QTAVYPVRSA YPQQSPYAQQ GTYYTQPLYA APPHVIHHTT
121 VVQPNGMPAT VYPAPIPPPR GNGVTMGMVA GTTMAMSAGT LLTAHSPTPV APHPVTVPTY
181 RAPGTPTYSY VPPQWLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FAM168B 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
- 2
- Mean surface accessibility (rSASA)
- 0.71
- Highest tissue expression
- 64 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 64 nTPM
- cerebral cortex: 61 nTPM
- skeletal muscle: 57 nTPM
- cerebellum: 55 nTPM
- amygdala: 50 nTPM
- tongue: 49 nTPM
Single-cell type
- rod photoreceptor cells: 136 nCPM
- myonuclei: 131 nCPM
- cone photoreceptor cells: 116 nCPM
- neutrophils: 112 nCPM
- endometrial glandular cells: 111 nCPM
- renal collecting duct intercalated cells: 108 nCPM
Immune cell
- naive CD4 T-cell: 4.8 nTPM
- gdT-cell: 4.4 nTPM
- eosinophil: 4.3 nTPM
- MAIT T-cell: 4 nTPM
- memory CD4 T-cell: 3.7 nTPM
- memory CD8 T-cell: 3.7 nTPM
Brain region
- basal ganglia: 113 nTPM
- thalamus: 102 nTPM
- cerebral cortex: 92 nTPM
- hippocampal formation: 90 nTPM
- spinal cord: 89 nTPM
- amygdala: 89 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)
- 1.09
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 1.27
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- none
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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FAM168B 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 FAM168B as an antibody target. Whether an autoantibody or antibody against FAM168B could matter depends on whether native FAM168B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FAM168B is annotated at the cell surface, where native FAM168B 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 FAM168B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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