Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
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Molecular interactions
External references
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ID 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: 84,482,601-84,700,463 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 6 transcripts (splice variants), 214 orthologues and is associated with 11 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000076159.3	Rttn-202	7178	2233aa	ENSRNOP00000068057.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MJA7	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,
ENSRNOT00000161351.1	Rttn-204	7643	2202aa	ENSRNOP00000106106.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000172044.1	Rttn-206	7316	2210aa	ENSRNOP00000102856.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000144544.1	Rttn-203	7238	2184aa	ENSRNOP00000112188.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000167449.1	Rttn-205	6953	2096aa	ENSRNOP00000102969.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000058160.7	Rttn-201	6942	2185aa	ENSRNOP00000054965.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZS92	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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