Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: SLC9B2 ENSDARG00000052700

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Description

solute carrier family 9 member B1 [Source:HGNC Symbol;Acc:HGNC:24244]

Location

Chromosome 1: 43,695,033-43,727,613 reverse strand.

GRCz11:CM002885.2

About this gene

This gene has 2 transcripts (splice variants) and 308 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000074600.6	SLC9B2-201	2252	564aa	ENSDARP00000069088.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M2B6Y3	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,
ENSDART00000181792.1	SLC9B2-202	4007	253aa	ENSDARP00000152451.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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