Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: slc5a9 ENSDARG00000005518

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Description

solute carrier family 5 member 9 [Source:NCBI gene (formerly Entrezgene);Acc:564815]

Location

Chromosome 8: 15,254,564-15,268,932 forward strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants), 215 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000024433.9	slc5a9-201	2188	657aa	ENSDARP00000008333.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A8WHP3	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, 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,
ENSDART00000141185.2	slc5a9-202	522	116aa	ENSDARP00000117713.1	Nonsense mediated decay	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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