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
External references
Supporting evidence
ID History
- Gene history

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Gene: CHD9 ENSPTRG00000008113

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Description

chromodomain helicase DNA binding protein 9 [Source:VGNC Symbol;Acc:VGNC:5734]

Location

Chromosome 16: 43,744,695-43,931,105 forward strand.

Pan_tro_3.0:CM000330.3

About this gene

This gene has 3 transcripts (splice variants), 217 orthologues and 32 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000014955.6	CHD9-201	11788	2898aa	ENSPTRP00000013848.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8MWW0 A0A6D2WLM6	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,
ENSPTRT00000083705.1	CHD9-203	2892	963aa	ENSPTRP00000086656.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TCQ6 A0A6D2Y186	-
ENSPTRT00000097801.1	CHD9-202	1374	457aa	ENSPTRP00000080147.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3ST76	-

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Summary

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