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: Pcnt ENSRNOG00000001276

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Description

pericentrin [Source:RGD Symbol;Acc:1595865]

Gene Synonyms

LOC309692

Location

Primary_assembly 20: 12,192,353-12,278,178 forward strand.

GRCr8:CM070410.1

About this gene

This gene has 4 transcripts (splice variants), 161 orthologues, 1 paralogue and is associated with 18 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000137564.1	Pcnt-203	9364	2921aa	ENSRNOP00000104628.1	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,
ENSRNOT00000097925.2	Pcnt-202	9346	2915aa	ENSRNOP00000095505.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ANK0	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,
ENSRNOT00000048218.8	Pcnt-201	9166	2855aa	ENSRNOP00000039329.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZMY8	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,
ENSRNOT00000152977.1	Pcnt-204	9013	2804aa	ENSRNOP00000100724.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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