Mus musculus Gene: Rcn2
Summary
InnateDB Gene IDBG-168462.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Rcn2
Gene Name reticulocalbin 2
Synonyms AA408742; Tcbp49
Species Mus musculus
Ensembl Gene ENSMUSG00000032320
Encoded Proteins
reticulocalbin 2
reticulocalbin 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000117906:
The protein encoded by this gene is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. This gene maps to the same region as type 4 Bardet-Biedl syndrome, suggesting a possible causative role for this gene in the disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 9:56041845-56061882
Strand Forward strand
Band B
Transcripts
ENSMUST00000114276 ENSMUSP00000109915
ENSMUST00000147842 ENSMUSP00000120953
ENSMUST00000151585
ENSMUST00000144869
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 13 experimentally validated interaction(s) in this database.
They are also associated with 23 interaction(s) predicted by orthology.
Experimentally validated
Total 13 [view]
Protein-Protein 13 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 23 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005509 calcium ion binding
GO:0005515 protein binding
Biological Process
Cellular Component
GO:0005730 nucleolus
GO:0005783 endoplasmic reticulum
GO:0005788 endoplasmic reticulum lumen
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q8BP92
TrEMBL Q3TE95
UniProt Splice Variant
Entrez Gene 26611
UniGene Mm.1782 Mm.402664
RefSeq NM_011992
OMIM
CCDS CCDS23206
HPRD
IMGT
MGI ID MGI:1349765
MGI Symbol Rcn2
EMBL AF049125 AK077486 AK169765 BC132320 BC145668
GenPept AAC05132 AAI32321 AAI45669 BAC36825 BAE41353
RNA Seq Atlas 26611