Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: RASL11B ENSPTRG00000016058

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Description

RAS like family 11 member B [Source:VGNC Symbol;Acc:VGNC:7425]

Location

Chromosome 4: 77,852,042-77,856,563 reverse strand.

Pan_tro_3.0:CM000318.3

About this gene

This gene has 1 transcript (splice variant), 199 orthologues and 43 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000029931.4	RASL11B-201	1971	248aa	ENSPTRP00000027621.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W2Y8 K7B2E1	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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