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

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Gene: C22orf23 ENSPTRG00000014355

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Description

chromosome 22 C22orf23 homolog [Source:VGNC Symbol;Acc:VGNC:5232]

Location

Chromosome 22: 24,487,709-24,497,757 reverse strand.

Pan_tro_3.0:CM000335.3

About this gene

This gene has 2 transcripts (splice variants) and 184 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000026824.5	C22orf23-202	1444	217aa	ENSPTRP00000024725.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8LNY0 A0A6D2Y6N5	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,
ENSPTRT00000077408.1	C22orf23-201	1381	196aa	ENSPTRP00000085997.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T9U1 A0A6D2WXS7	-

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Summary

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