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: SLC37A2 ENSBTAG00000016704

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Description

solute carrier family 37 member 2 [Source:VGNC Symbol;Acc:VGNC:34843]

Location

Primary_assembly 29: 28,495,844-28,523,735 forward strand.

ARS-UCD1.3:CM008196.2

About this gene

This gene has 3 transcripts (splice variants), 238 orthologues, 12 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000069229.2	SLC37A2-201	1746	505aa	ENSBTAP00000063485.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M1A8	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 P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,
ENSBTAT00000022208.7	SLC37A2-202	2960	501aa	ENSBTAP00000022208.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DIQ9	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSBTAT00000083825.2	SLC37A2-203	1449	482aa	ENSBTAP00000062264.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LYD9	-

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Summary

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