Homo sapiens Gene: CHP1
Summary
InnateDB Gene IDBG-6990.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CHP1
Gene Name calcineurin-like EF hand protein 1
Synonyms CHP; p22; p24; Sid470p; SLC9A1BP
Species Homo sapiens
Ensembl Gene ENSG00000187446
Encoded Proteins
Calcium-binding protein p22
Calcium-binding protein p22
Calcium-binding protein p22
Calcium-binding protein p22
Calcium-binding protein p22
Calcium-binding protein p22
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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]
Gene Information
Type Protein coding
Genomic Location Chromosome 15:41230839-41281890
Strand Forward strand
Band q15.1
Transcripts
ENST00000334660 ENSP00000335632
ENST00000392151 ENSP00000440490
ENST00000558351
ENST00000560411 ENSP00000453375
ENST00000560784 ENSP00000452772
ENST00000561280
ENST00000560397 ENSP00000454007
ENST00000560633
ENST00000560965 ENSP00000453392
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
Experimentally validated
Total 10 [view]
Protein-Protein 9 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0004860 protein kinase inhibitor activity
GO:0005215 transporter activity
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0008017 microtubule binding
GO:0015459 potassium channel regulator activity
GO:0019900 kinase binding
GO:0048306 calcium-dependent protein binding
Biological Process
GO:0001578 microtubule bundle formation
GO:0001933 negative regulation of protein phosphorylation
GO:0006469 negative regulation of protein kinase activity
GO:0006611 protein export from nucleus
GO:0006813 potassium ion transport
GO:0007264 small GTPase mediated signal transduction
GO:0010923 negative regulation of phosphatase activity
GO:0017156 calcium ion-dependent exocytosis
GO:0022406 membrane docking
GO:0031122 cytoplasmic microtubule organization
GO:0031397 negative regulation of protein ubiquitination
GO:0031953 negative regulation of protein autophosphorylation
GO:0032088 negative regulation of NF-kappaB transcription factor activity
GO:0032417 positive regulation of sodium:proton antiporter activity
GO:0042308 negative regulation of protein import into nucleus
GO:0045056 transcytosis
GO:0050821 protein stabilization
GO:0051222 positive regulation of protein transport
GO:0051259 protein oligomerization
GO:0051453 regulation of intracellular pH
GO:0060050 positive regulation of protein glycosylation
GO:0061024 membrane organization
GO:0061025 membrane fusion
GO:0070885 negative regulation of calcineurin-NFAT signaling cascade
GO:0071468 cellular response to acidity
GO:0090314 positive regulation of protein targeting to membrane
Cellular Component
GO:0000139 Golgi membrane
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005783 endoplasmic reticulum
GO:0005793 endoplasmic reticulum-Golgi intermediate compartment
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0015630 microtubule cytoskeleton
GO:0030133 transport vesicle
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Hyaluronan uptake and degradation pathway
Mucopolysaccharidoses pathway
Myoclonic epilepsy of Lafora pathway
Defective B4GALT7 causes EDS, progeroid type pathway
Defective CHST6 causes MCDC1 pathway
MPS VI - Maroteaux-Lamy syndrome pathway
Defective PAPSS2 causes SEMD-PA pathway
Metabolism of carbohydrates pathway
MPS IIID - Sanfilippo syndrome D pathway
Defective SLC26A2 causes chondrodysplasias pathway
MPS IX - Natowicz syndrome pathway
Defective EXT1 causes exostoses 1, TRPS2 and CHDS pathway
Defective CHST14 causes EDS, musculocontractural type pathway
MPS IV - Morquio syndrome B pathway
Defective B3GAT3 causes JDSSDHD pathway
Defective CHST3 causes SEDCJD pathway
MPS IV - Morquio syndrome A pathway
Defective EXT2 causes exostoses 2 pathway
Diseases associated with glycosaminoglycan metabolism pathway
MPS II - Hunter syndrome pathway
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) pathway
Glycosaminoglycan metabolism pathway
Diseases of glycosylation pathway
MPS VII - Sly syndrome pathway
Defective CHSY1 causes TPBS pathway
Metabolism pathway
MPS I - Hurler syndrome pathway
MPS IIIA - Sanfilippo syndrome A pathway
Hyaluronan metabolism pathway
MPS IIIC - Sanfilippo syndrome C pathway
Disease pathway
Glycogen storage diseases pathway
MPS IIIB - Sanfilippo syndrome B pathway
KEGG
INOH
PID NCI
Calcium signaling in the CD4+ TCR pathway
Role of Calcineurin-dependent NFAT signaling in lymphocytes
Cross-References
SwissProt
TrEMBL F5GX29
UniProt Splice Variant
Entrez Gene 11261
UniGene Hs.623717 Hs.732259
RefSeq NM_007236
HUGO HGNC:17433
OMIM 606988
CCDS CCDS10073
HPRD 06101
IMGT
EMBL AC012652
GenPept
RNA Seq Atlas 11261