Loading…

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

Configure this page

Share this page

Bookmark this page

.

Gene: CXorf22 ENSG00000165164

.

Description

chromosome X open reading frame 22 [Source:HGNC Symbol;Acc:28546]

Gene Synonyms

MGC34831

Location

Chromosome X: 35,937,851-36,008,269 forward strand.

GRCh37:CM000685.1

About this gene

This gene has 2 transcripts (splice variants) and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000297866.5	CXorf22-001	3608	976aa	ENSP00000297866.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS14237	Q6ZTR5	NM_152632.3	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000493930.1	CXorf22-002	3468	754aa	ENSP00000433564.1	Nonsense mediated decay		Q6ZTR5	-	-

.

Summary

.

.