Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: CHCT1 ENSMMUG00000016565

Description

CHD1 helical C-terminal domain containing 1 [Source:VGNC Symbol;Acc:VGNC:70410]

Gene Synonyms

C16H17ORF64

Location

Mmul_10:CM014351.1

About this gene

This gene has 1 transcript (splice variant) and 114 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMMUT00000023262.4	CHCT1-201	1228	236aa	ENSMMUP00000021763.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8J8XHA7 F6VXL1	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,

Summary