Mus musculus Gene: 4933433P14Rik
Summary
InnateDB Gene IDBG-169578.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol 4933433P14Rik
Gene Name RIKEN cDNA 4933433P14 gene
Synonyms 4933433P14Rik
Species Mus musculus
Ensembl Gene ENSMUSG00000044715
Encoded Proteins
RIKEN cDNA 4933433P14 gene
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 ENSG00000100744:
This gene encodes a protein that is involved as a negative regulator of GSK3-beta in the Wnt signaling pathway. The encoded protein may play a role in the retinoic acid signaling pathway by regulating the functional interactions between GSK3-beta, beta-catenin and cyclin D1, and it regulates the beta-catenin/N-cadherin pool. The encoded protein contains a GSK3-beta interacting domain (GID) in its C-terminus, which is similar to the GID of Axin. The protein also contains an evolutionarily conserved RII-binding domain, which facilitates binding with protein kinase-A and GSK3-beta, enabling its role as an A-kinase anchoring protein. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 12:105685352-105703047
Strand Forward strand
Band E
Transcripts
ENSMUST00000051934 ENSMUSP00000057939
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 8 interaction(s) predicted by orthology.
Predicted by orthology
Total 8 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0008150 biological_process
Cellular Component
GO:0005575 cellular_component
GO:0048471 perinuclear region of cytoplasm
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q8BGR8
TrEMBL Q3TBR1
UniProt Splice Variant
Entrez Gene 66787
UniGene Mm.248019 Mm.400230 Mm.412306
RefSeq NM_178613
OMIM
CCDS CCDS49161
HPRD
IMGT
MGI ID MGI:1914037
MGI Symbol Gskip
EMBL AK029484 AK042664 AK079775 AK168962 AK171097 BC031494 CH466549
GenPept AAH31494 BAC26470 BAC31325 BAC37748 BAE40767 BAE42246 EDL18753
RNA Seq Atlas 66787