Gene: Bsnd ENSMUSG00000025418

Description

barttin CLCNK type accessory beta subunit [Source:MGI Symbol;Acc:MGI:2153465]

Gene Synonyms

Bartter syndrome, infantile, with sensorineural deafness (Barttin)

Location

GRCm39:CM000997.3

About this gene

This gene has 1 transcript (splice variant), 115 orthologues and is associated with 18 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000054472.4	Bsnd-201	2756	307aa	ENSMUSP00000049563.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS18419	Q8VIM4	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

Summary