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: rfx6 ENSDARG00000041702

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Description

regulatory factor X6 [Source:HGNC Symbol;Acc:HGNC:21478]

Location

Chromosome 20: 42,506,612-42,534,504 reverse strand.

GRCz11:CM002904.2

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues, 8 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000132310.4	rfx6-202	2749	907aa	ENSDARP00000116051.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000061122.4	rfx6-201	2547	848aa	ENSDARP00000061121.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5RJA1	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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