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: Molecular function
- GO: Cellular component
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: Prr29 ENSRNOG00000060193

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Description

proline rich 29 [Source:RGD Symbol;Acc:1307288]

Gene Synonyms

LOC287761, RGD1307288

Location

Primary_assembly 10: 91,805,650-91,810,213 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 3 transcripts (splice variants) and 68 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000078446.3	Prr29-201	3080	187aa	ENSRNOP00000074239.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K7K1	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,
ENSRNOT00000145401.1	Prr29-202	2859	107aa	ENSRNOP00000106866.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000157472.1	Prr29-203	1584	183aa	ENSRNOP00000104108.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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