Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: raph1b ENSDARG00000061732

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Description

Ras association (RalGDS/AF-6) and pleckstrin homology domains 1b [Source:NCBI gene (formerly Entrezgene);Acc:560319]

Location

Chromosome 1: 29,664,336-29,743,640 forward strand.

GRCz11:CM002885.2

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000088290.7	raph1b-201	6134	1511aa	ENSDARP00000082723.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QZE7	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,
ENSDART00000154342.3	raph1b-203	4086	925aa	ENSDARP00000128517.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSDART00000136066.2	raph1b-202	614	161aa	ENSDARP00000118277.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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