Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Rab1b ENSRNOG00000050510

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Description

RAB1B, member RAS oncogene family [Source:RGD Symbol;Acc:1642882]

Gene Synonyms

MGC105830, Rab1bl

Location

Primary_assembly X: 50,857,916-50,859,762 forward strand.

mRatBN7.2:CM026994.1

About this gene

This gene has 1 transcript (splice variant), 237 orthologues and 71 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000042711.5	Rab1b-201	1847	201aa	ENSRNOP00000067788.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V6H0	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,

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Summary

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