Gene: Slc10a6 ENSMUSG00000029321

Description

solute carrier family 10 (sodium/bile acid cotransporter family), member 6 [Source:MGI Symbol;Acc:MGI:1923000]

Gene Synonyms

8430417G17Rik

Location

Chromosome 5: 103,753,575-103,777,401 reverse strand.

GRCm39:CM000998.3

About this gene

This gene has 4 transcripts (splice variants), 118 orthologues, 6 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000031263.2	Slc10a6-201	2124	373aa	ENSMUSP00000031263.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS19477	Q9CXB2	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000532517.1	Slc10a6-202	2503	210aa	ENSMUSP00000310880.1	Nonsense mediated decay		-	-
ENSMUST00000532518.1	Slc10a6-203	1838	99aa	ENSMUSP00000310881.1	Nonsense mediated decay		-	-
ENSMUST00000532519.1	Slc10a6-204	1785	189aa	ENSMUSP00000310882.1	Nonsense mediated decay		-	-

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Gene: Slc10a6 ENSMUSG00000029321

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Gene: Slc10a6 ENSMUSG00000029321

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