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: slc20a2 ENSDARG00000060796

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Description

solute carrier family 20 member 2 [Source:ZFIN;Acc:ZDB-GENE-060929-828]

Gene Synonyms

fi23g11, wu:fi23g11, zgc:152990

Location

Chromosome 8: 29,770,098-29,851,706 reverse strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants), 222 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000149297.3	slc20a2-201	7816	662aa	ENSDARP00000124436.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q836	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,
ENSDART00000167487.2	slc20a2-202	2807	662aa	ENSDARP00000139221.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q836	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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