CHP1
Calcineurin B homologous protein 1
Also known as: CHP, CHP1_HUMAN, p22, p24, Sid470p, SLC9A1BP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99653
- Gene
- CHP1
- Ensembl
- ENSG00000187446
- Chromosome
- 15
- Canonical length
- 195 aa
- Protein class
- Disease related genes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Transporters
- Subcellular location
- Vesicles
OverviewNCBI Gene
This gene encodes a phosphoprotein that binds to the Na+/H+ exchanger NHE1. This protein serves as an essential cofactor which supports the physiological activity of NHE family members and may play a role in the mitogenic regulation of NHE1. The protein shares similarity with calcineurin B and calmodulin and it is also known to be an endogenous inhibitor of calcineurin activity. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
195 residues, UniProt reviewed canonical sequence.
>Q99653|CHP1
1 MGSRASTLLR DEELEEIKKE TGFSHSQITR LYSRFTSLDK GENGTLSRED FQRIPELAIN
61 PLGDRIINAF FPEGEDQVNF RGFMRTLAHF RPIEDNEKSK DVNGPEPLNS RSNKLHFAFR
121 LYDLDKDEKI SRDELLQVLR MMVGVNISDE QLGSIADRTI QEADQDGDSA ISFTEFVKVL
181 EKVDVEQKMS IRFLHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CHP1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 173 nTPM
Expression across tissuesHPA
Tissue
- liver: 173 nTPM
- colon: 107 nTPM
- stomach: 106 nTPM
- tongue: 81 nTPM
- duodenum: 80 nTPM
- skeletal muscle: 79 nTPM
Single-cell type
- esophageal apical cells: 923 nCPM
- parietal cells: 824 nCPM
- enterocytes: 494 nCPM
- colonocytes: 443 nCPM
- hepatocytes: 418 nCPM
- gastric chief cells: 320 nCPM
Immune cell
- eosinophil: 275 nTPM
- basophil: 256 nTPM
- classical monocyte: 227 nTPM
- non-classical monocyte: 208 nTPM
- intermediate monocyte: 204 nTPM
- neutrophil: 173 nTPM
Brain region
- pons: 89 nTPM
- hypothalamus: 82 nTPM
- medulla oblongata: 82 nTPM
- midbrain: 78 nTPM
- hippocampal formation: 75 nTPM
- white matter: 72 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CHP1.
Disease | AllUniProt
Conditions CHP1 is implicated in, by any mechanism.
- Spastic ataxia 9, autosomal recessive (SPAX9) MIM:618438
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 11 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Spastic ataxia 9, autosomal recessive
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)
- 0.54
- gnomAD pLI
- 0.63
- gnomAD missense Z
- 2.26
- DepMap mean gene effect
- -0.18
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to acidic pH
- cytoplasmic microtubule organization
- membrane fusion
- membrane organization
- microtubule bundle formation
- negative regulation of calcineurin-NFAT signaling cascade
- negative regulation of NF-kappaB transcription factor activity
- negative regulation of phosphatase activity
- negative regulation of protein autophosphorylation
- negative regulation of protein import into nucleus
- negative regulation of protein kinase activity
- negative regulation of protein phosphorylation
- negative regulation of protein ubiquitination
- positive regulation of glycoprotein biosynthetic process
- positive regulation of phospholipid biosynthetic process
- positive regulation of protein targeting to membrane
- positive regulation of protein transport
- positive regulation of sodium:proton antiporter activity
- potassium ion transport
- protein export from nucleus
- protein stabilization
- regulation of intracellular pH
- small GTPase-mediated signal transduction
- membrane docking
Molecular functions
- calcium ion binding
- calcium-dependent protein binding
- kinase binding
- microtubule binding
- potassium channel regulator activity
- protein kinase inhibitor activity
- sodium:proton antiporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CHP1 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 CHP1 as an antibody target. Whether an autoantibody or antibody against CHP1 could matter depends on whether native CHP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CHP1 is annotated at the cell surface, where native CHP1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label CHP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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