FAM86B2
Putative protein N-methyltransferase FAM86B2
Also known as: F86B2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P0C5J1
- Gene
- FAM86B2
- Ensembl
- ENSG00000145002
- Chromosome
- 8
- Canonical length
- 330 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Predicted to enable protein-lysine N-methyltransferase activity. Predicted to be involved in methylation. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
330 residues, UniProt reviewed canonical sequence.
>P0C5J1|FAM86B2
1 MAPEENAGTE LLLQGFERRF LAVRTLRSFP WQSLEAKLRD SSDSELLRDI LQKTVRHPVC
61 VKHPPSVKYA WCFLSELIKK HEAVHTEPLD KLYEVLAETL MAKESTQGHR SYLLSSGGSV
121 TLSKSTAIIS HGTTGLVTWD AALYLAEWAI ENPAAFINRT VLELGSGAGL TGLAICKMCR
181 PRAYIFSDPH SRILEQLRGN VLLNGLSLEA DITGNLDSPR VTVAQLDWDV AMVHQLSAFQ
241 PDVVIAADVL YCPEAIVSLV GVLQRLAACR EHKRAPEVYV AFTVRNPETC QLFTTELGRD
301 GIRWEAEAHH DQKLFPYGEH LEMAMLNLTLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FAM86B2 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)
- 0.26
- Highest tissue expression
- 0.5 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 0.5 nTPM
- pituitary gland: 0.5 nTPM
- parathyroid gland: 0.4 nTPM
- skin: 0.4 nTPM
- basal ganglia: 0.3 nTPM
- fallopian tube: 0.3 nTPM
Single-cell type
- gonadotrophs: 1.5 nCPM
- adrenal cortex cells: 0.9 nCPM
- cardiomyocytes: 0.9 nCPM
- epididymal principal cells: 0.8 nCPM
- fallopian tube ciliated cells: 0.8 nCPM
- thyrotrophs: 0.8 nCPM
Immune cell
- T-reg: 0.4 nTPM
- MAIT T-cell: 0.2 nTPM
- memory CD8 T-cell: 0.2 nTPM
- intermediate monocyte: 0.1 nTPM
- memory CD4 T-cell: 0.1 nTPM
- myeloid DC: 0.1 nTPM
Brain region
- thalamus: 0.4 nTPM
- basal ganglia: 0.3 nTPM
- cerebral cortex: 0.3 nTPM
- hippocampal formation: 0.3 nTPM
- midbrain: 0.3 nTPM
- pons: 0.3 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)
- 1.74
- gnomAD pLI
- 0
- gnomAD missense Z
- -2.39
- DepMap mean gene effect
- -0.06
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FAM86B2 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 FAM86B2 as an antibody target. Whether an autoantibody or antibody against FAM86B2 could matter depends on whether native FAM86B2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FAM86B2 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 FAM86B2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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