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: slc22a13b ENSDARG00000059166

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Description

solute carrier family 22 member 13b [Source:NCBI gene (formerly Entrezgene);Acc:556601]

Location

Chromosome 24: 20,006,711-20,016,817 reverse strand.

GRCz11:CM002908.2

About this gene

This gene has 3 transcripts (splice variants), 331 orthologues and 24 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000082201.6	slc22a13b-201	1871	542aa	ENSDARP00000076638.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FCW8	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,
ENSDART00000189448.1	slc22a13b-203	1321	415aa	ENSDARP00000152835.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q08BI5	-
ENSDART00000164243.2	slc22a13b-202	210	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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