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Cancer Genome Characterization Initiative

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Gene Info

Gene Information For:Mm. Bsnd, Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Sequence ID:NM_080458
Entrez Gene ID:140475
Ensembl ID:ENSMUSG00000025418

Database Links

UniGeneEntrez GeneEnsembl GeneVegaSNPSNP: GeneViewSNP: VarViewAssemblies

Gene Expression Data


Cytogenetic Location (from UniGene)

Cytogenetic Location:4 C7|4

Chromosomal Position (from UCSC)

Chromosomal Position:4: 106483461 - 106492243

NM_080458 exon info from UCSC:

Transcript StartTranscript EndChromosomal Start Chromosomal End
31990106156062106158049
19912245106159188106159442
22462337106160583106160674
23382716106164469106164847

Full-Length MGC Clones for This Gene

IMAGE IdStatusAccession GenBank Def Line
4221532Full LengthBC038287Bartter syndrome, infantile, with sensorineural deafness (Barttin)

Protein Infomation

RefSeq
mRNAProteinSwissProtPfam
NM_080458 NP_536706 Q8VIM4  

Related Sequences

 
mRNAGenPeptSwissProt
BC038287 AAH38287 Q8VIM4
AF391088 AAL33907 Q8VIM4
AY373833 AAQ81629 Q8VIM4
AK052587 BAC35049 Q8VIM4

Homologs (from HomoloGene)
Note: Both orthologs and paralogs are included.
Organism Symbol Protein Homolog Similarity
(% aa unchanged)
Organism Symbol Entrez
Gene
Gene Info Protein
M.musculus Bsnd NP_536706 R.norvegicus Bsnd 192675   NP_620435 88
H.sapiens BSND 7809 Gene Info NP_476517 74

Gene Ontology
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)