Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: selenot1a ENSDARG00000058354

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Description

selenoprotein T, 1a [Source:ZFIN;Acc:ZDB-GENE-030327-6]

Gene Synonyms

cb700, selt1a, sept1a, wu:fb63h09, wu:fc79a12

Location

Chromosome 2: 9,684,305-9,696,283 reverse strand.

GRCz11:CM002886.2

About this gene

This gene has 1 transcript (splice variant), 217 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000165712.2	selenot1a-201	1301	193aa	ENSDARP00000136996.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q802F2	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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Summary

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