Homo sapiens Gene: KBTBD13
Summary
InnateDB Gene IDBG-304083.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol KBTBD13
Gene Name kelch repeat and BTB (POZ) domain containing 13
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000234438
Encoded Proteins
kelch repeat and BTB (POZ) domain containing 13
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The gene belongs to a family of genes encoding proteins containing a BTB domain and several kelch repeats. The BTB domain functions as a protein-protein interaction module, which includes an ability to self-associate or to interact with non-BTB domain-containing proteins. The kelch motif typically occurs in groups of five to seven repeats, and has been found in proteins with diverse functions. Known functions of these family members include transcription regulation, ion channel tetramerization and gating, protein ubiquitination or degradation, and cytoskeleton regulation. The exact function of this family member has yet to be determined. [provided by RefSeq, Jun 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 15:65076816-65078192
Strand Forward strand
Band q22.31
Transcripts
ENST00000432196 ENSP00000388723
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0016567 protein ubiquitination
Cellular Component
GO:0005737 cytoplasm
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 C9JR72
TrEMBL
UniProt Splice Variant
Entrez Gene 390594
UniGene Hs.586890
RefSeq NM_001101362
HUGO HGNC:37227
OMIM 613727
CCDS CCDS45281
HPRD
IMGT
EMBL AC013553 CH471082
GenPept EAW77711
RNA Seq Atlas 390594