CTNNB1
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesCTNNB1, CTNNB, MRD19, armadillo, catenin beta 1, EVR7, NEDSDV
External IDsOMIM: 116806 HomoloGene: 1434 GeneCards: CTNNB1
Genetically Related Diseases
colorectal cancer, pilomatrixoma, autosomal dominant non-syndromic intellectual disability 19, exudative vitreoretinopathy 7, liver carcinoma, cerebellar medulloblastoma[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001098209
NM_001098210
NM_001904
NM_001330729

n/a

RefSeq (protein)

NP_001091679
NP_001091680
NP_001317658
NP_001895

n/a

Location (UCSC)Chr 3: 41.19 – 41.26 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Long list of GO for testing

  1. ^ "Diseases that are genetically associated with CTNNB1 view/edit references on wikidata".
  2. ^ "Human PubMed Reference:".