ZNF22: Zinc Finger Protein 22 (KOX 15) - Gene Overview

A comprehensive biomedical resource for ZNF22, a C2H2-type zinc finger transcription factor involved in development and cancer.

Gene Information Card

Symbol ZNF22
Full Name zinc finger protein 22 (KOX 15)
Gene Type protein-coding
Chromosomal Location 10q11.22
NCBI Gene ID 7570 ncbi.nlm.nih.gov/gene/7570
Ensembl ID ENSG00000198752
UniProt ID P17026
OMIM ID 194533
HGNC ID 13035
Aliases KOX15, ZNF22L, ZNF22P

Description

ZNF22 (zinc finger protein 22) is a protein-coding gene located on chromosome 10q11.22. It encodes a C2H2-type zinc finger transcription factor, also known as KOX 15, which is involved in transcriptional regulation. ZNF22 is expressed in various tissues and has been implicated in developmental processes and cancer, particularly through its role in the Wnt signaling pathway.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal cancer ZNF22 overexpression may activate Wnt/β-catenin signaling, promoting tumorigenesis. PMID: 23455423
Hepatocellular carcinoma ZNF22 upregulation correlates with poor prognosis and increased cell proliferation. PMID: 28708995
Gastric cancer ZNF22 expression is elevated and associated with lymph node metastasis. PMID: 27158336

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 12.5 Medium
Bone marrow 8.2 Low
Lymph node 6.1 Low
Brain 4.3 Low
Liver 3.8 Low
Cell Line Expression
Cell Line nTPM Notes
K562 (leukemia) 15.2 High expression
HepG2 (liver cancer) 10.1 Moderate expression
HeLa (cervical cancer) 7.4 Low expression
A549 (lung cancer) 5.6 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.101C>T (p.Pro34Leu) Missense <0.1% Unknown functional impact
c.205G>A (p.Gly69Ser) Missense <0.1% Reported in COSMIC; potential loss of DNA binding
c.328_330del (p.Lys110del) In-frame deletion <0.1% Reported in COSMIC; may alter zinc finger structure
Mutation functional classification

Loss of Function (LOF)

Missense mutations in zinc finger domains (e.g., p.Gly69Ser) may impair DNA binding and transcriptional activity.

Gain of Function (GOF)

Overexpression of wild-type ZNF22 in cancer suggests a potential gain-of-function role via Wnt pathway activation.

Dominant Negative (DN)

No dominant-negative mutations have been characterized for ZNF22.

Pathways

Wnt signaling pathway (Reactome: R-HSA-201681)
Transcriptional regulation by zinc finger proteins (Reactome: R-HSA-212436)

Protein Summary

ZNF22 encodes a 306-amino acid protein containing 12 C2H2-type zinc finger domains, characteristic of transcription factors. It localizes to the nucleus and binds DNA to regulate gene expression. ZNF22 is known to interact with TCF/LEF transcription factors and modulate Wnt/β-catenin signaling. Its expression is dysregulated in several cancers, suggesting a role in tumor progression.

Related Products

Product name Cat.No. Species Gene ID
ZNF22 Knockout HEK293 Cell Line EDJ-KQ5315 Human 7570 Details Get a Quote
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ZNF221 Knockout HEK293 Cell Line EDJ-KQ6061 Human 7638 Details Get a Quote
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ZNF224 Knockout HEK293 Cell Line EDJ-KQ6108 Human 7767 Details Get a Quote
ZNF226 Knockout HEK293 Cell Line EDJ-KQ6110 Human 7769 Details Get a Quote
ZNF225 Knockout HEK293 Cell Line EDJ-KQ6112 Human 7768 Details Get a Quote
ZNF227 Knockout HEK293 Cell Line EDJ-KQ6115 Human 7770 Details Get a Quote
ZNF224 Knockout HCT 116 Cell Line EDJ-KQ28549 Human 7767 Details Get a Quote
ZNF22 Knockout A-549 Cell Line EDJ-KQ29673 Human 7570 Details Get a Quote
ZNF22 Knockout HCT 116 Cell Line EDJ-KQ29674 Human 7570 Details Get a Quote
ZNF22 Knockout HeLa Cell Line EDJ-KQ29675 Human 7570 Details Get a Quote
ZNF221 Knockout A-549 Cell Line EDJ-KQ29749 Human 7638 Details Get a Quote
ZNF221 Knockout HCT 116 Cell Line EDJ-KQ29750 Human 7638 Details Get a Quote
Displaying Records 1 To 15 Of 36 Records
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