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

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Gene: rasgef1bb ENSDARG00000044251

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Description

RasGEF domain family, member 1Bb [Source:NCBI gene;Acc:445085]

Gene Synonyms

fc34e01, im:7136415, rasgef, wu:fc34e01, zgc:91814

Location

Chromosome 10: 9,159,279-9,184,667 forward strand.

GRCz11:CM002894.2

About this gene

This gene has 1 transcript (splice variant), 204 orthologues and 27 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000064968.5	rasgef1bb-201	2173	475aa	ENSDARP00000064967.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6DBW1	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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