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: Biological process
- GO: Cellular component
- GO: Molecular function
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: Pxdc1 ENSRNOG00000017093

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Description

PX domain containing 1 [Source:RGD Symbol;Acc:1311307]

Gene Synonyms

LOC361238, MGC116297, RGD1311307

Location

Primary_assembly 17: 30,481,373-30,510,331 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 2 transcripts (splice variants) and 207 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000060143.4	Pxdc1-201	2193	251aa	ENSRNOP00000056888.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2UMR7	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,
ENSRNOT00000108422.2	Pxdc1-202	2277	231aa	ENSRNOP00000081377.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZSE8 A6J7F6 Q4KLK8	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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