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

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Gene: slc9a6b ENSDARG00000075382

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Description

solute carrier family 9 member 6b [Source:ZFIN;Acc:ZDB-GENE-080226-2]

Gene Synonyms

nhe6

Location

Chromosome 10: 26,571,174-26,597,800 forward strand.

GRCz11:CM002894.2

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000112956.3	slc9a6b-201	3712	692aa	ENSDARP00000099786.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R354	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,
ENSDART00000148617.3	slc9a6b-202	1698	559aa	ENSDARP00000123753.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F8W586	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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