Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
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: Pcid2 ENSRNOG00000025222

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Description

PCI domain containing 2 [Source:RGD Symbol;Acc:1307041]

Gene Synonyms

LOC361182, RGD1307041

Location

Primary_assembly 16: 83,124,658-83,156,970 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000135871.1	Pcid2-203	1792	414aa	ENSRNOP00000108750.1	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,
ENSRNOT00000116016.2	Pcid2-202	3072	391aa	ENSRNOP00000082024.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZTF8	-
ENSRNOT00000044085.6	Pcid2-201	2364	399aa	ENSRNOP00000049378.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MAF5	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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