TFB2M
Dimethyladenosine transferase 2, mitochondrial
Also known as: FLJ22661, FLJ23182, Hkp1, TFB2M_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H5Q4
- Gene
- TFB2M
- Ensembl
- ENSG00000162851
- Chromosome
- 1
- Canonical length
- 396 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables mitochondrial transcription factor activity. Involved in transcription initiation at mitochondrial promoter. Located in mitochondrial nucleoid. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
396 residues, UniProt reviewed canonical sequence.
>Q9H5Q4|TFB2M
1 MWIPVVGLPR RLRLSALAGA GRFCILGSEA ATRKHLPARN HCGLSDSSPQ LWPEPDFRNP
61 PRKASKASLD FKRYVTDRRL AETLAQIYLG KPSRPPHLLL ECNPGPGILT QALLEAGAKV
121 VALESDKTFI PHLESLGKNL DGKLRVIHCD FFKLDPRSGG VIKPPAMSSR GLFKNLGIEA
181 VPWTADIPLK VVGMFPSRGE KRALWKLAYD LYSCTSIYKF GRIEVNMFIG EKEFQKLMAD
241 PGNPDLYHVL SVIWQLACEI KVLHMEPWSS FDIYTRKGPL ENPKRRELLD QLQQKLYLIQ
301 MIPRQNLFTK NLTPMNYNIF FHLLKHCFGR RSATVIDHLR SLTPLDARDI LMQIGKQEDE
361 KVVNMHPQDF KTLFETIERS KDCAYKWLYD ETLEDRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TFB2M 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)
- 0.34
- Highest tissue expression
- 35 nTPM
Expression across tissuesHPA
Tissue
- liver: 35 nTPM
- bone marrow: 23 nTPM
- tongue: 23 nTPM
- skeletal muscle: 22 nTPM
- adrenal gland: 22 nTPM
- kidney: 20 nTPM
Single-cell type
- oocytes: 83 nCPM
- basal keratinocytes: 60 nCPM
- gastric progenitor cells: 58 nCPM
- endometrial glandular cells: 53 nCPM
- suprabasal keratinocytes: 44 nCPM
- differentiating spermatogonia: 43 nCPM
Immune cell
- NK-cell: 15 nTPM
- myeloid DC: 13 nTPM
- T-reg: 12 nTPM
- naive B-cell: 12 nTPM
- memory B-cell: 12 nTPM
- MAIT T-cell: 12 nTPM
Brain region
- choroid plexus: 12 nTPM
- cerebellum: 11 nTPM
- cerebral cortex: 6.7 nTPM
- white matter: 6.7 nTPM
- hypothalamus: 6.5 nTPM
- spinal cord: 6.4 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)
- 0.95
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.12
- DepMap mean gene effect
- -0.59
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 13% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- mitochondrial transcription factor activity
- RNA binding
- rRNA (adenine-N6,N6-)-dimethyltransferase activity
- rRNA (adenine-N6-)-methyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TFB2M 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 TFB2M as an antibody target. Whether an autoantibody or antibody against TFB2M could matter depends on whether native TFB2M is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TFB2M 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 TFB2M as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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