Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Pls3 ENSRNOG00000027520

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Description

plastin 3 [Source:RGD Symbol;Acc:621409]

Location

Primary_assembly X: 116,401,293-116,495,893 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 4 transcripts (splice variants), 262 orthologues, 2 paralogues and is associated with 12 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000162443.1	Pls3-204	3207	661aa	ENSRNOP00000109117.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000158329.1	Pls3-203	3181	630aa	ENSRNOP00000107822.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KGB3	-
ENSRNOT00000139298.1	Pls3-202	3163	634aa	ENSRNOP00000100088.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000060168.4	Pls3-201	3116	639aa	ENSRNOP00000056912.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LPK7	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data