Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
146227
Gene name Gene Name - the full gene name approved by the HGNC.
Brain expressed associated with NEDD4 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BEAN1
Synonyms (NCBI Gene) Gene synonyms aliases
BEAN, SCA31
Disease Acronyms (UniProt) Disease acronyms from UniProt database
SCA31
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16q21
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612051 24160 ENSG00000166546
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Nystagmus Nystagmus rs137852207, rs137852208, rs1928435502, rs137852209, rs137852210, rs1929191668, rs137852211, rs137852212, rs2124209414, rs387906720, rs387906721, rs1602791884, rs786205896
Spinocerebellar ataxia SPINOCEREBELLAR ATAXIA 31 (disorder), Spinocerebellar ataxia type 31 rs80356538, rs80356539, rs56144125, rs28937887, rs80356544, rs80356540, rs80356542, rs1941485201, rs121918306, rs151344520, rs151344519, rs151344521, rs151344523, rs151344512, rs193922926
View all (203 more)
19878914, 17611710, 22992774
Associations from Text Mining
Disease Name Relationship Type References
Ataxia Associate 21088341
Spinocerebellar Ataxia 31 Associate 19878914, 30634945