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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: DHX9 ENSPTRG00000001759

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Description

DExH-box helicase 9 [Source:VGNC Symbol;Acc:VGNC:6745]

Location

Chromosome 1: 161,407,238-161,455,936 forward strand.

Pan_tro_3.0:CM000314.3

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000003191.6	DHX9-201	4305	1270aa	ENSPTRP00000002937.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XD23 H2Q0R0	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,
ENSPTRT00000091059.1	DHX9-202	1302	433aa	ENSPTRP00000088269.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3THC3	-

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Summary

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