ZNF222: Zinc Finger Protein 222

A Krüppel-associated box (KRAB) domain-containing zinc finger transcription factor with potential roles in transcriptional regulation and cancer.

Gene Information Card

Symbol ZNF222
Full Name zinc finger protein 222
Gene Type protein-coding
Chromosomal Location 19q13.43
NCBI Gene ID 7573 ncbi.nlm.nih.gov/gene/7573
Ensembl ID ENSG00000167552
UniProt ID Q9UK13
OMIM ID None
HGNC ID 13036
Aliases ZNF222, ZNF222_HUMAN, FLJ32115

Description

ZNF222 (zinc finger protein 222) is a protein-coding gene located on chromosome 19q13.43. It encodes a member of the Krüppel C2H2-type zinc finger protein family, characterized by a KRAB (Krüppel-associated box) domain at the N-terminus and multiple C2H2 zinc finger motifs. The protein is predicted to function as a transcription factor involved in transcriptional repression. Expression data suggest broad but low-level expression across many tissues. The gene has been implicated in various cancers, including breast and lung cancer, through mutation and expression analyses.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Altered expression and somatic mutations may contribute to tumorigenesis via dysregulation of target genes. COSMIC; literature
Lung cancer Somatic mutations and copy number alterations observed in lung adenocarcinoma samples. COSMIC; literature
Colorectal cancer Mutations reported in colorectal cancer cell lines and primary tumors. COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 2.3 Low
Brain 1.1 Low
Lung 0.8 Low
Breast 0.6 Low
Colon 0.5 Low
Cell Line Expression
Cell Line nTPM Notes
MCF7 (breast cancer) 0.9 Low expression
A549 (lung cancer) 0.7 Low expression
HCT116 (colorectal cancer) 0.6 Low expression
HEK293 (embryonic kidney) 1.2 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.100C>T (p.Arg34Cys) Missense <0.1% Unknown; predicted possibly damaging
c.250G>A (p.Gly84Ser) Missense <0.1% Unknown; predicted benign
c.400_401insA Frameshift <0.1% Predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift mutations (e.g., c.400_401insA) are predicted to cause premature truncation and loss of zinc finger domains, likely resulting in loss of DNA-binding and transcriptional repression activity.

Gain of Function (GOF)

No evidence for gain-of-function mutations in ZNF222.

Dominant Negative (DN)

No evidence for dominant-negative mutations in ZNF222.

Pathways

No specific pathways curated in Reactome or KEGG for ZNF222.

Protein Summary

ZNF222 is a 532-amino acid protein containing a KRAB domain (residues 1-75) and 12 C2H2-type zinc finger motifs (residues 100-520). The KRAB domain mediates transcriptional repression through recruitment of co-repressors such as KAP1/TRIM28. The zinc fingers are predicted to bind specific DNA sequences, though target genes remain largely unknown. The protein localizes to the nucleus and is expressed at low levels in most tissues. Structural predictions indicate a multi-zinc finger array typical of KRAB-ZNF transcription factors.

Related Products

Product name Cat.No. Species Gene ID
ZNF222 Knockout HEK293 Cell Line EDJ-KQ6069 Human 7673 Details Get a Quote
ZNF222 Knockout A-549 Cell Line EDJ-KQ29766 Human 7673 Details Get a Quote
ZNF222 Knockout HCT 116 Cell Line EDJ-KQ29767 Human 7673 Details Get a Quote
ZNF222 Knockout HeLa Cell Line EDJ-KQ29768 Human 7673 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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