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: slc22a7b.2 ENSDARG00000091252

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Description

solute carrier family 22 member 7b, tandem duplicate 2 [Source:ZFIN;Acc:ZDB-GENE-030131-9391]

Gene Synonyms

fj67g09, oat2c, si:ch211-183f23.3, wu:fj67g09

Location

Chromosome 17: 21,994,043-22,001,935 reverse strand.

GRCz11:CM002901.2

About this gene

This gene has 3 transcripts (splice variants), 249 orthologues and 24 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000122190.4	slc22a7b.2-201	2606	471aa	ENSDARP00000105434.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FED9	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,
ENSDART00000193302.1	slc22a7b.2-203	1599	401aa	ENSDARP00000149301.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8Q857	-
ENSDART00000185429.1	slc22a7b.2-202	1509	371aa	ENSDARP00000144655.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8Q1V7	-

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Summary

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