Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: LOC120094289 ENSRNOG00000056476

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Description

solute carrier family 22 member 13-like [Source:RGD Symbol;Acc:41095427]

Location

Primary_assembly 8: 127,800,097-127,811,724 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 329 orthologues, 25 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000104015.2	LOC120094289-202	1689	562aa	ENSRNOP00000088097.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A5H4	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,
ENSRNOT00000078303.3	LOC120094289-201	1974	551aa	ENSRNOP00000075628.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B2GV36	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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Paralogues

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