Gene Gene information from NCBI Gene database.
Entrez ID 146227
Gene name Brain expressed associated with NEDD4 1
Gene symbol BEAN1
Synonyms (NCBI Gene)
BEANSCA31
Chromosome 16
Chromosome location 16q21
Summary The protein encoded by this gene is one of several proteins that interact with NEDD4, a member of a family of ubiquitin-protein ligases. These proteins have PY motifs in common that bind to the WW domains of NEDD4. NEDD4 is developmentally regulated, and
miRNA miRNA information provided by mirtarbase database.
23
miRTarBase ID miRNA Experiments Reference
MIRT820639 hsa-miR-3134 CLIP-seq
MIRT820640 hsa-miR-3688-3p CLIP-seq
MIRT820641 hsa-miR-4520a-5p CLIP-seq
MIRT820642 hsa-miR-4520b-5p CLIP-seq
MIRT820643 hsa-miR-4534 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612051 24160 ENSG00000166546
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q3B7T3
Protein name Protein BEAN1 (Brain-expressed protein associating with Nedd4 homolog) (BEAN)
Family and domains
Sequence
MSFKRPCPLARYNRTSYFYPTFSESSEHSHLLVSPVLVASAVIGVVIILSCITIIVGSIR
RDRQARLQRHRHRHHRHHHHHHHHRRRRHREYEHGYVSDEHTYSRSSRRMRYACSSSEDW
PPPLDISSDGDVDATVLRELYPDSPPGYEECVGPGATQLYVPTDAPPPYSLTDSCPTLDG
TSDSGSGHSPGRHQQEQRTPAQGGLHTVSMDTLPPYEAVCGAGPPSGLLPLPGPDPGPRG
SQGSPTPTRAPASGPERIV
Sequence length 259
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Spinocerebellar ataxia  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
9
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
BEAN1-related disorder Likely benign; Benign rs141546513, rs527873790, rs72788593, rs564817056, rs146861397, rs115852696, rs779019822, rs911363927 RCV003929200
RCV003923909
RCV003929740
RCV003963924
RCV003949408
RCV003979157
RCV003971488
RCV003967098
Spinocerebellar ataxia type 31 Benign rs529552966 RCV004579667
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Ataxia Associate 21088341
Spinocerebellar Ataxia 31 Associate 19878914, 30634945