Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Ppwd1 ENSRNOG00000012505

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Description

peptidylprolyl isomerase domain and WD repeat containing 1 [Source:RGD Symbol;Acc:1310204]

Gene Synonyms

LOC294711, RGD1310204

Location

Primary_assembly 2: 37,071,083-37,094,242 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 195 orthologues and 24 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000016863.7	Ppwd1-201	2453	646aa	ENSRNOP00000016863.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I5F6 D3ZVP6	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 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,
ENSRNOT00000103323.2	Ppwd1-202	2294	639aa	ENSRNOP00000081682.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZSQ6	-

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Summary

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