Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- 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: Plcxd1 ENSRNOG00000049866

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Description

phosphatidylinositol-specific phospholipase C, X domain containing 1 [Source:RGD Symbol;Acc:1560935]

Gene Synonyms

LOC100909600, LOC304575, RGD1560935

Location

Primary_assembly 12: 52,238,623-52,241,865 reverse strand.

GRCr8:CM070402.1

About this gene

This gene has 1 transcript (splice variant), 219 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000073986.4	Plcxd1-201	1325	307aa	ENSRNOP00000064541.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J2E2 M0R583	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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