Homo sapiens Gene: CNN3
Summary
InnateDB Gene IDBG-100388.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CNN3
Gene Name calponin 3, acidic
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000117519
Encoded Proteins
calponin 3, acidic
calponin 3, acidic
calponin 3, acidic
calponin 3, acidic
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a protein with a markedly acidic C terminus; the basic N-terminus is highly homologous to the N-terminus of a related gene, CNN1. Members of the CNN gene family all contain similar tandemly repeated motifs. This encoded protein is associated with the cytoskeleton but is not involved in contraction. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:94896949-94927278
Strand Reverse strand
Band p21.3
Transcripts
ENST00000370206 ENSP00000359225
ENST00000394202 ENSP00000377752
ENST00000415017 ENSP00000401452
ENST00000461018
ENST00000487539
ENST00000474409
ENST00000545882 ENSP00000440081
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Experimentally validated
Total 5 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003779 actin binding
GO:0005515 protein binding
GO:0005516 calmodulin binding
Biological Process
GO:0030855 epithelial cell differentiation
GO:0031032 actomyosin structure organization
Cellular Component
GO:0005575 cellular_component
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL E9PDU6 Q9BWY6
UniProt Splice Variant
Entrez Gene 1266
UniGene Hs.483454
RefSeq NM_001839 NM_001286056 NM_001286055 XM_006710335
HUGO HGNC:2157
OMIM 602374
CCDS CCDS30775 CCDS65592 CCDS65593
HPRD 03848
IMGT
EMBL AC093429 AC105942 AL359554
GenPept CAC36092
RNA Seq Atlas 1266