Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Prr16 ENSRNOG00000019744

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Description

proline rich 16 [Source:RGD Symbol;Acc:1564528]

Gene Synonyms

LOC103694214, LOC361327, RGD1564528

Location

Primary_assembly 18: 46,623,058-46,830,385 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 5 transcripts (splice variants), 199 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000100979.2	Prr16-202	2907	359aa	ENSRNOP00000076470.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A107	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,
ENSRNOT00000125728.1	Prr16-204	2919	235aa	ENSRNOP00000111817.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000026724.6	Prr16-201	2702	312aa	ENSRNOP00000026724.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A107	-
ENSRNOT00000148587.1	Prr16-205	2214	235aa	ENSRNOP00000100063.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000118503.2	Prr16-203	1265	305aa	ENSRNOP00000087158.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A7G3 A6IX11	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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