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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Slc13a2 ENSRNOG00000010337

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Description

solute carrier family 13 member 2 [Source:RGD Symbol;Acc:61920]

Gene Synonyms

Nadc1, naDC-1

Location

Primary_assembly 10: 63,789,876-63,817,184 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 261 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000038690.6	Slc13a2-201	2428	587aa	ENSRNOP00000038185.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P70545	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,

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Summary

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