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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Slc16a14 ENSRNOG00000017072

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Description

solute carrier family 16, member 14 [Source:RGD Symbol;Acc:1309675]

Gene Synonyms

LOC316578

Location

Primary_assembly 9: 93,558,144-93,585,396 reverse strand.

GRCr8:CM070399.1

About this gene

This gene has 1 transcript (splice variant), 172 orthologues and 12 paralogues.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000064875.3	Slc16a14-201	5308	512aa	ENSRNOP00000061785.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JWD4 D4A0E5	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,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data