Homo sapiens Protein: BICC1
Summary
InnateDB Protein IDBP-75035.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BICC1
Protein Name bicaudal C homolog 1 (Drosophila)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000362993
InnateDB Gene IDBG-75033 (BICC1)
Protein Structure
UniProt Annotation
Function Putative RNA-binding protein. Acts as a negative regulator of Wnt signaling. May be involved in regulating gene expression during embryonic development. {ECO:0000269PubMed:21922595}.
Subcellular Localization Cytoplasm {ECO:0000250}.
Disease Associations Renal dysplasia, cystic (CYSRD) [MIM:601331]: An anomaly of the kidney characterized by numerous renal cysts and apparent disorder of differentiation of the renal parenchyma. Kidney of affected individuals lack the normal renal bean shape, and the collection drainage system. The cystic, dysplastic kidney contains undifferentiated mesenchyme, cartilaginous tissue, and immature collecting ducts. {ECO:0000269PubMed:21922595}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003723 RNA binding
GO:0005515 protein binding
GO:0044822 poly(A) RNA binding
Biological Process
GO:0007275 multicellular organismal development
GO:0090090 negative regulation of canonical Wnt signaling pathway
Cellular Component
GO:0005737 cytoplasm
Protein Structure and Domains
PDB ID
InterPro IPR001660 Sterile alpha motif domain
IPR004087 K Homology domain
IPR004088 K Homology domain, type 1
IPR011510 Sterile alpha motif, type 2
IPR013761 Sterile alpha motif/pointed domain
IPR021129 Sterile alpha motif, type 1
PFAM PF00013
PF13014
PF07647
PF00536
PRINTS
PIRSF
SMART SM00454
SM00322
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9H694
PhosphoSite PhosphoSite-Q9H694
TrEMBL
UniProt Splice Variant
Entrez Gene 80114
UniGene Hs.633222
RefSeq NP_001073981
HUGO HGNC:19351
OMIM 614295
CCDS CCDS31206
HPRD
IMGT
EMBL AK026129 AY726586
GenPept BAB15369