MYBPH
Myosin-binding protein H
Also known as: MYBPH_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13203
- Gene
- MYBPH
- Ensembl
- ENSG00000133055
- Chromosome
- 1
- Canonical length
- 477 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Mitochondria
OverviewNCBI Gene
Predicted to be a structural constituent of muscle. Predicted to be involved in sarcomere organization. Predicted to be located in myosin filament. Predicted to be active in M band. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
477 residues, UniProt reviewed canonical sequence.
>Q13203|MYBPH
1 MMEKNTSEGP ACSPEETASE SAKVPTAEPP GEVAVSESTR EEQVPKPQAP APQAPTASTA
61 TKPAPPSEDV PSAPLLLTLD DVSSSSVTVS WEPPERLGRL GLQGYVLELC REGASEWVPV
121 SARPMMVTQQ TVRNLALGDK FLLRVSAVSS AGAGPPAMLD QPIHIRENIE APKIRVPRHL
181 RQTYIRQVGE TVNLQIPFQG KPKPQATWTH NGHALDSQRV SMRTGDQDSI LFIRSAQRSD
241 SGRYELTVRV EDLEAKAVID ILVIEKPGPP SSIRLLDVWG CNAALQWTPP QDTGNTELLG
301 YMVQKADKKT GQWFTVLERY HPTTCTISDL IIGNSYSFRV FSENLCGLST SATVTKELAH
361 IQKADIAAKP KGFIERDFSE APSFTQPLAD HTSTPGYSTQ LFCSVRASPK PKIIWMKNKM
421 EIQGNPKYRA LSEQGVCTLE IRKPSPFDSG VYTCKAINVL GEASVDCRLE VKASAAHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MYBPH 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)
- 0.36
- Highest tissue expression
- 73 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 73 nTPM
- tongue: 18 nTPM
- salivary gland: 17 nTPM
- choroid plexus: 4.9 nTPM
- liver: 4.7 nTPM
- prostate: 3.1 nTPM
Single-cell type
- thymic myoid cells: 393 nCPM
- myonuclei: 6.7 nCPM
- podocytes: 6.2 nCPM
- pdcs: 2.5 nCPM
- microglia: 1.9 nCPM
- breast secretory cells: 1.3 nCPM
Immune cell
- plasmacytoid DC: 2.5 nTPM
- intermediate monocyte: 0.4 nTPM
- non-classical monocyte: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- pons: 12 nTPM
- thalamus: 12 nTPM
- cerebral cortex: 9.7 nTPM
- medulla oblongata: 8.9 nTPM
- midbrain: 8.8 nTPM
- basal ganglia: 8.4 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)
- 1.28
- 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 3% 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
- Immunoglobulin subtype 2
- Immunoglobulin domain subtype
- Fibronectin type III
- Immunoglobulin-like domain
- Immunoglobulin I-set
- Immunoglobulin-like fold
- Fibronectin type III superfamily
- Immunoglobulin-like domain superfamily
- Striated Muscle Structural and Regulatory Protein
- Fibronectin type III domain
- Immunoglobulin I-set domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MYBPH as an antibody target. Whether an autoantibody or antibody against MYBPH could matter depends on whether native MYBPH is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MYBPH 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 MYBPH as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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