Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
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External references
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ID History
- Gene history

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Gene: sel-12 WBGene00004769

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Description

Presenilin sel-12 [Source:NCBI gene (formerly Entrezgene);Acc:180441]

Location

Chromosome X: 915,867-918,290 forward strand.

WBcel235:BX284606.5

About this gene

This gene has 1 transcript (splice variant) and 405 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
F35H12.3.1	sel-12-201	1473	444aa	F35H12.3.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P52166	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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