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: Slc16a9 ENSRNOG00000049063

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Description

solute carrier family 16, member 9 [Source:RGD Symbol;Acc:1596295]

Gene Synonyms

AABR07044759.1, LOC687808, MCT 9

Location

Primary_assembly 20: 18,334,946-18,376,195 reverse strand.

GRCr8:CM070410.1

About this gene

This gene has 2 transcripts (splice variants), 272 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000074657.4	Slc16a9-201	3919	508aa	ENSRNOP00000067303.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RCI4	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,
ENSRNOT00000173735.1	Slc16a9-202	3665	460aa	ENSRNOP00000110019.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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