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: slc8a2b ENSDARG00000100592

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Description

solute carrier family 8 member 2b [Source:ZFIN;Acc:ZDB-GENE-050419-209]

Gene Synonyms

ncx2b, si:dkeyp-109h9.1

Location

Chromosome 15: 42,767,803-42,981,467 forward strand.

GRCz11:CM002899.2

About this gene

This gene has 2 transcripts (splice variants), 72 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000164879.2	slc8a2b-201	3458	961aa	ENSDARP00000132805.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B2CZC4	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,
ENSDART00000167763.2	slc8a2b-202	2529	842aa	ENSDARP00000133162.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1LVA9	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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