Entity Details

Primary name BICC1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9H694
EntryNameBICC1_HUMAN
FullNameProtein bicaudal C homolog 1
TaxID9606
Evidenceevidence at protein level
Length974
SequenceStatuscomplete
DateCreated2006-12-12
DateModified2021-06-02

Ontological Relatives

GenesBICC1

GO terms

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GOName
GO:0001822 kidney development
GO:0003723 RNA binding
GO:0005737 cytoplasm
GO:0007368 determination of left/right symmetry
GO:0007507 heart development
GO:0090090 negative regulation of canonical Wnt signaling pathway

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR001660 Sterile alpha motif domainDomainDomain
IPR004087 K Homology domainDomainDomain
IPR004088 K Homology domain, type 1DomainDomain
IPR013761 Sterile alpha motif/pointed domain superfamilyFamilyHomologous superfamily
IPR036612 K Homology domain, type 1 superfamilyFamilyHomologous superfamily
IPR037974 BICC1, SAM domainDomainDomain

Diseases

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Disease IDSourceNameDescription
601331 OMIMRenal dysplasia, cystic (CYSRD)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. Disease susceptibility is associated with variants affecting the gene represented in this entry.