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: slc25a36a ENSDARG00000038731

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Description

solute carrier family 25 member 36a [Source:NCBI gene;Acc:436940]

Gene Synonyms

zgc:92447

Location

Chromosome 2: 39,731,284-39,759,059 reverse strand.

GRCz11:CM002886.2

About this gene

This gene has 3 transcripts (splice variants), 262 orthologues and 64 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000007333.11	slc25a36a-201	4657	311aa	ENSDARP00000004962.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B2GNU1 Q6DG32	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,
ENSDART00000148135.3	slc25a36a-203	730	97aa	ENSDARP00000140604.1	Nonsense mediated decay	A0A0R4IYK0	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000138424.2	slc25a36a-202	803	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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