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

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Pdcd10 ENSRNOG00000010147

.

Description

programmed cell death 10 [Source:RGD Symbol;Acc:1359329]

Gene Synonyms

MGC72992

Location

Primary_assembly 2: 162,602,516-162,644,612 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 275 orthologues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000013585.6	Pdcd10-201	1385	212aa	ENSRNOP00000013585.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2UIL5	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,
ENSRNOT00000103849.2	Pdcd10-202	1151	201aa	ENSRNOP00000093534.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AJ47	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,

.

Orthologues

.

.