Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Ren ENSRNOG00000002937

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Description

renin [Source:RGD Symbol;Acc:3554]

Gene Synonyms

Ren1

Location

Primary_assembly 13: 47,348,143-47,359,543 forward strand.

GRCr8:CM070403.1

About this gene

This gene has 2 transcripts (splice variants), 220 orthologues, 8 paralogues and is associated with 79 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000003951.6	Ren-201	1590	402aa	ENSRNOP00000003951.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IC75 P08424	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,
ENSRNOT00000097884.2	Ren-202	1389	396aa	ENSRNOP00000094943.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ANY3	-

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Summary

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