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

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Gene: CHD1 ENSSSCG00000014177

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Description

chromodomain helicase DNA binding protein 1 [Source:VGNC Symbol;Acc:VGNC:86629]

Location

Primary_assembly 2: 105,113,668-105,203,119 reverse strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues and 30 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000032432.4	CHD1-202	7856	1706aa	ENSSSCP00000023979.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5K1VUK9 A0A8D0T1D7	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,
ENSSSCT00000015489.5	CHD1-201	7222	1691aa	ENSSSCP00000015079.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0T7K4 A0A8D1QJW5	-

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Paralogues

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