Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: SLC22A16 ENSBTAG00000010507

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Description

solute carrier family 22 member 16 [Source:VGNC Symbol;Acc:VGNC:34724]

Location

Primary_assembly 9: 39,753,094-39,788,294 forward strand.

ARS-UCD2.0:CM008176.2

About this gene

This gene has 2 transcripts (splice variants), 256 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000028664.5	SLC22A16-201	1950	572aa	ENSBTAP00000028664.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q17QN9	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,
ENSBTAT00000068635.2	SLC22A16-202	1872	567aa	ENSBTAP00000062246.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LQ29	-

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Summary

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