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: Slc2a12 ENSRNOG00000011161

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Description

solute carrier family 2 member 12 [Source:RGD Symbol;Acc:1310175]

Gene Synonyms

LOC308028

Location

Primary_assembly 1: 24,589,707-24,694,290 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 288 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116309.2	Slc2a12-202	4220	645aa	ENSRNOP00000087966.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A9T2	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,
ENSRNOT00000167074.1	Slc2a12-204	4311	602aa	ENSRNOP00000107616.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000015566.7	Slc2a12-201	3901	607aa	ENSRNOP00000015566.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZNG4	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,
ENSRNOT00000127461.1	Slc2a12-203	1953	588aa	ENSRNOP00000112347.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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