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

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Gene: C22H3orf20 ENSBTAG00000040133

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Description

chromosome 22 C3orf20 homolog [Source:VGNC Symbol;Acc:VGNC:49183]

Location

Primary_assembly 22: 57,544,168-57,595,868 reverse strand.

ARS-UCD1.3:CM008189.2

About this gene

This gene has 1 transcript (splice variant), 122 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000008930.6	C22H3orf20-201	3453	908aa	ENSBTAP00000008930.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BJV2	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,

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Summary

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