Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: Psen1 ENSRNOG00000009110

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Description

presenilin 1 [Source:RGD Symbol;Acc:3425]

Gene Synonyms

PS-1

Location

Primary_assembly 6: 109,060,352-109,106,189 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 1 transcript (splice variant), 200 orthologues, 1 paralogue and is associated with 36 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000012495.9	Psen1-201	6211	468aa	ENSRNOP00000012495.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JDR2 P97887	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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