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

Gene: C22H22orf31 ENSPTRG00000014213

Description

chromosome 22 C22orf31 homolog [Source:VGNC Symbol;Acc:VGNC:5234]

Location

Pan_tro_3.0:CM000335.3

About this gene

This gene has 2 transcripts (splice variants) and 72 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000026549.3	C22H22orf31-202	873	290aa	ENSPTRP00000024467.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XB88 H2QLF6	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,
ENSPTRT00000089920.1	C22H22orf31-201	1720	289aa	ENSPTRP00000062547.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RD29	-

Summary