Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: PCP2 ENSBTAG00000008906

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Description

Purkinje cell protein 2 [Source:VGNC Symbol;Acc:VGNC:32644]

Location

Primary_assembly 7: 16,476,406-16,483,428 reverse strand.

ARS-UCD2.0:CM008174.2

About this gene

This gene has 4 transcripts (splice variants) and 106 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000121409.1	PCP2-204	849	259aa	ENSBTAP00000097008.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TJB0	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000093582.2	PCP2-203	893	217aa	ENSBTAP00000077641.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RYF5	-
ENSBTAT00000011725.5	PCP2-201	481	126aa	ENSBTAP00000011725.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A1A4P3	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSBTAT00000129002.1	PCP2-202	469	134aa	ENSBTAP00000100229.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TUI8	-

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Summary

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