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

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Gene: Rab6a ENSRNOG00000018176

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Description

RAB6A, member RAS onco family [Source:RGD Symbol;Acc:619737]

Gene Synonyms

RCO4-3, Rab6, Rab6b, rab-6

Location

Primary_assembly 1: 164,369,861-164,417,763 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 198 orthologues and 64 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000164517.1	Rab6a-203	1333	211aa	ENSRNOP00000104096.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000025104.8	Rab6a-201	3556	208aa	ENSRNOP00000025104.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H2UHP9 A6I6Q3 Q9WVB1	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSRNOT00000106849.2	Rab6a-202	3424	208aa	ENSRNOP00000091495.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AFQ7 A6I6Q2	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,

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Summary

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