Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
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

Gene: C22H3orf49 ENSBTAG00000039133

Description

chromosome 22 C3orf49 homolog [Source:VGNC Symbol;Acc:VGNC:59323]

Location

ARS-UCD1.3:CM008189.2

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSBTAT00000053491.3	C22H3orf49-201	1280	No protein	-	A gene that has homology to known protein-coding genes but contain a frameshift and/or stop codon(s) which disrupts the ORF. Thought to have arisen through duplication followed by loss of function.Pseudogene	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