Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Slc26a10 ENSRNOG00000029465

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Description

solute carrier family 26, member 10 [Source:RGD Symbol;Acc:1564851]

Gene Synonyms

LOC366909, RGD1564851

Location

Primary_assembly 7: 64,880,699-64,889,409 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 185 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000052288.7	Slc26a10-201	3137	690aa	ENSRNOP00000049501.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZXL0	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 ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSRNOT00000113632.2	Slc26a10-202	3119	684aa	ENSRNOP00000091854.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GJX7	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,

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Summary

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