FAM13C
Protein FAM13C
Also known as: FA13C_HUMAN, FAM13C1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NE31
- Gene
- FAM13C
- Ensembl
- ENSG00000148541
- Chromosome
- 10
- Canonical length
- 585 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
No narrative summary is available for FAM13C in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
585 residues, UniProt reviewed canonical sequence.
>Q8NE31|FAM13C
1 MFSCFCFSLQ DNSFSSTTVT ECDEDPVSLH EDQTDCSSLR DENNKENYPD AGALVEEHAP
61 PSWEPQQQNV EATVLVDSVL RPSMGNFKSR KPKSIFKAES GRSHGESQET EHVVSSQSEC
121 QVRAGTPAHE SPQNNAFKCQ ETVRLQPRID QRTAISPKDA FETRQDLNEE EAAQVHGVKD
181 PAPASTQSVL ADGTDSADPS PVHKDGQNEA DSAPEDLHSV GTSRLLYHIT DGDNPLLSPR
241 CSIFSQSQRF NLDPESAPSP PSTQQFMMPR SSSRCSCGDG KEPQTITQLT KHIQSLKRKI
301 RKFEEKFEQE KKYRPSHGDK TSNPEVLKWM NDLAKGRKQL KELKLKLSEE QGSAPKGPPR
361 NLLCEQPTVP RENGKPEAAG PEPSSSGEET PDAALTCLKE RREQLPPQED SKVTKQDKNL
421 IKPLYDRYRI IKQILSTPSL IPTIQEEEDS DEDRPQGSQQ PSLADPASHL PVGDHLTYSN
481 ETEPVRALLP DEKKEVKPPA LSMSNLHEAT MPVLLDHLRE TRADKKRLRK ALREFEEQFF
541 KQTGRSPQKE DRIPMADEYY EYKHIKAKLR LLEVLISKQD VAKTILocalizationUniProt · AlphaFold · HPA
Whether an antibody against FAM13C 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.61
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 38 nTPM
- midbrain: 26 nTPM
- cerebral cortex: 22 nTPM
- tongue: 21 nTPM
- hippocampal formation: 19 nTPM
- amygdala: 17 nTPM
Single-cell type
- oligodendrocytes: 572 nCPM
- renal collecting duct intercalated cells: 269 nCPM
- salivary ionocytes: 249 nCPM
- prostatic glandular cells: 181 nCPM
- pericytes: 158 nCPM
- thymic myoid cells: 158 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 152 nTPM
- medulla oblongata: 120 nTPM
- basal ganglia: 110 nTPM
- pons: 96 nTPM
- thalamus: 94 nTPM
- midbrain: 92 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)
- 0.63
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.76
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FAM13C as an antibody target. Whether an autoantibody or antibody against FAM13C could matter depends on whether native FAM13C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FAM13C 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 FAM13C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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