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

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Gene: slc12a9 ENSDARG00000060366

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Description

solute carrier family 12 member 9 [Source:NCBI gene;Acc:793341]

Gene Synonyms

fk87c04, im:7146124, si:ch211-284e13.1, wu:fk87c04

Location

Chromosome 5: 38,215,924-38,248,462 reverse strand.

GRCz11:CM002889.2

About this gene

This gene has 2 transcripts (splice variants), 184 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000139479.3	slc12a9-202	4466	899aa	ENSDARP00000120278.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A2BFP5	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,
ENSDART00000084917.5	slc12a9-201	2987	899aa	ENSDARP00000079352.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A2BFP5	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,

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Summary

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