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

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Gene: RIT1 ENSBTAG00000000105

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Description

Ras like without CAAX 1 [Source:VGNC Symbol;Acc:VGNC:33987]

Location

Primary_assembly 3: 14,853,235-14,862,512 forward strand.

ARS-UCD2.0:CM008170.2

About this gene

This gene has 2 transcripts (splice variants), 155 orthologues and 37 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000123937.2	RIT1-202	3555	296aa	ENSBTAP00000100190.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TNQ2	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,
ENSBTAT00000000114.6	RIT1-201	3300	219aa	ENSBTAP00000000114.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6RAN8	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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