C3orf22

Chromosome 3 Open Reading Frame 22

Gene Information Card

Symbol C3orf22
Full Name chromosome 3 open reading frame 22
Gene Type protein-coding
Chromosomal Location 3q13.2
NCBI Gene ID 84971 ncbi.nlm.nih.gov/gene/84971
Ensembl ID ENSG00000163739
UniProt ID Q8N6T3
OMIM ID 617437
HGNC ID 26779
Aliases FLJ22662, MGC131891

Description

C3orf22 (chromosome 3 open reading frame 22) is a protein-coding gene located on the long arm of chromosome 3 (3q13.2). The encoded protein has no well-characterized function and is not associated with any known disease or pathway. Expression data suggest low to moderate levels in certain tissues, but the biological role remains largely unknown.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
No disease associations Not established No evidence

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 2.5 Low
Thyroid 1.8 Low
Adrenal gland 1.2 Low
Other tissues <1.0 Not detected
Cell Line Expression
Cell Line nTPM Notes
HEK293 0.5 Low expression
HeLa 0.3 Low expression
K562 0.2 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
No reported variants N/A N/A N/A
Mutation functional classification

Loss of Function (LOF)

No data

Gain of Function (GOF)

No data

Dominant Negative (DN)

No data

Protein Summary

The C3orf22 protein (UniProt Q8N6T3) is a 244-amino acid polypeptide with no known domains or functional motifs. Its molecular function and cellular role remain uncharacterized.

Related Products

Product name Cat.No. Species Gene ID
C3orf22 Knockout HEK293 Cell Line EDJ-KQ11374 Human 152065 Details Get a Quote
C3orf22 Knockout HeLa Cell Line EDJ-KQ58700 Human 152065 Details Get a Quote
C3orf22 Knockout A-549 Cell Line EDJ-KQ67184 Human 152065 Details Get a Quote
C3orf22 Knockout HCT 116 Cell Line EDJ-KQ75587 Human 152065 Details Get a Quote
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