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: Cellular component
- GO: Molecular function
- GO: Biological process
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: Rttn ENSRNOG00000038200

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Description

rotatin [Source:RGD Symbol;Acc:1306706]

Gene Synonyms

LOC291377

Location

Primary_assembly 18: 82,221,050-82,398,333 forward strand.

mRatBN7.2:CM026991.1

About this gene

This gene has 2 transcripts (splice variants), 217 orthologues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000058160.6	Rttn-201	6997	2201aa	ENSRNOP00000054965.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZS92	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,
ENSRNOT00000076159.2	Rttn-202	7332	2060aa	ENSRNOP00000068057.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MJA7	-

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Summary

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