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: Rasl11b ENSRNOG00000002097

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Description

RAS-like family 11 member B [Source:RGD Symbol;Acc:1303099]

Location

Primary_assembly 14: 34,014,509-34,019,152 reverse strand.

mRatBN7.2:CM026987.1

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues, 41 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000104776.1	Rasl11b-202	1134	285aa	ENSRNOP00000097701.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GM65	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,
ENSRNOT00000002869.6	Rasl11b-201	1824	247aa	ENSRNOP00000002869.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6IMA7	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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