FAM110C
Protein FAM110C
Also known as: F110C_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q1W6H9
- Gene
- FAM110C
- Ensembl
- ENSG00000184731
- Chromosome
- 2
- Canonical length
- 321 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables alpha-tubulin binding activity. Involved in positive regulation of cell migration; positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and regulation of cell projection assembly. Located in cell cortex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
321 residues, UniProt reviewed canonical sequence.
>Q1W6H9|FAM110C
1 MRALAALSAP PNERLLPRDP AATRDPDAAR PARRSAVERL AADRAKYVRG RPGTGRGVAS
61 EGSGPGAIKC PGNDPGPPAR APAPVARRAI ARKPLRPDSL IIYRQKCEFV RGSGADGPRA
121 SLVKKLFQGP GKDKAPVPRT GDEGKAGNPE TVPTTPGPAA DPAIPETPAP AARSAAPSSV
181 PAAPPGPEPR VVRRRGLQRS QSDLSSRYSA ALAESDTFFQ YCGLDPEVVE ALGRENFTAG
241 SDCVTLKVRS VSVATSGSGF SRHSGGDDEG LQEEELIEQV PSTTSVIERN ARIIKWLYTC
301 KKAKETPSQE QSRTRGSKPS RLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FAM110C 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)
- 0.67
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 30 nTPM
- epididymis: 20 nTPM
- seminal vesicle: 19 nTPM
- liver: 16 nTPM
- vagina: 15 nTPM
- pancreas: 13 nTPM
Single-cell type
- epididymal basal cells: 327 nCPM
- esophageal apical cells: 262 nCPM
- endometrial luminal cells: 250 nCPM
- ocular epithelial cells: 210 nCPM
- endometrial glandular cells: 140 nCPM
- urothelial cells: 132 nCPM
Immune cell
- T-reg: 0.4 nTPM
- basophil: 0.1 nTPM
- neutrophil: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- choroid plexus: 9.2 nTPM
- basal ganglia: 9.1 nTPM
- cerebral cortex: 7.6 nTPM
- white matter: 5.8 nTPM
- amygdala: 5.2 nTPM
- hippocampal formation: 5.2 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)
- 1.86
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.33
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
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
Biological processes
- positive regulation of cell migration
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- regulation of cell projection assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FAM110C 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 FAM110C as an antibody target. Whether an autoantibody or antibody against FAM110C could matter depends on whether native FAM110C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FAM110C 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 FAM110C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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