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: RASSF9 ENSBTAG00000026966

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Description

Ras association domain family member 9 [Source:VGNC Symbol;Acc:VGNC:33765]

Location

Primary_assembly 5: 15,463,007-15,500,124 reverse strand.

ARS-UCD2.0:CM008172.2

About this gene

This gene has 2 transcripts (splice variants), 190 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000101268.1	RASSF9-201	6680	414aa	ENSBTAP00000089841.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1B705	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,
ENSBTAT00000038601.6	RASSF9-202	1756	414aa	ENSBTAP00000038414.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1B705	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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