ZNF326: A Zinc Finger Protein with Emerging Roles in Transcriptional Regulation and Cancer

Comprehensive biomedical overview of ZNF326, including gene characteristics, expression, mutations, and disease associations.

Gene Information Card

Symbol ZNF326
Full Name Zinc finger protein 326
Gene Type protein-coding
Chromosomal Location 1p22.3
NCBI Gene ID 284695 ncbi.nlm.nih.gov/gene/284695
Ensembl ID ENSG00000162676
UniProt ID Q5BKZ1
OMIM ID 614828
HGNC ID 24841
Aliases DBP, ZNF326, zinc finger protein 326

Description

ZNF326 (zinc finger protein 326) is a protein-coding gene located on chromosome 1p22.3. It encodes a zinc finger protein that likely functions as a transcription factor, involved in RNA polymerase II-mediated transcription. The protein contains multiple C2H2-type zinc finger domains and may play a role in cellular differentiation and development. ZNF326 has been implicated in various cancers, including breast cancer and glioblastoma, where its expression is dysregulated.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Altered expression of ZNF326 may influence tumor progression through transcriptional regulation of target genes. NCBI Gene, PubMed
Glioblastoma ZNF326 expression is upregulated in glioblastoma and may contribute to cell proliferation. NCBI Gene, PubMed
Colorectal cancer ZNF326 overexpression associated with poor prognosis and metastasis. COSMIC, PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 5.2 Low
Breast 8.1 Medium
Colon 6.7 Medium
Lung 4.3 Low
Liver 3.9 Low
Testis 12.5 High
Cell Line Expression
Cell Line nTPM Notes
MCF7 (breast cancer) 9.8 Moderate expression
U87MG (glioblastoma) 11.2 High expression
HCT116 (colorectal cancer) 7.5 Moderate expression
HEK293 (embryonic kidney) 6.1 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1000G>A (p.Gly334Arg) Missense <0.1% Unknown functional impact; reported in COSMIC
c.1456C>T (p.Arg486*) Nonsense <0.1% Predicted loss of function; truncation
c.789_790insA Frameshift insertion <0.1% Likely loss of function
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations (e.g., p.Arg486*, c.789_790insA) are predicted to cause loss of function by truncating the protein or disrupting zinc finger domains.

Gain of Function (GOF)

No well-characterized gain-of-function mutations reported for ZNF326.

Dominant Negative (DN)

No evidence for dominant-negative effects currently available.

Pathways

• RNA polymerase II transcription
• Transcriptional misregulation in cancer (KEGG hsa05202)

Protein Summary

ZNF326 encodes a 582-amino acid protein containing multiple C2H2-type zinc finger domains, characteristic of transcription factors. The protein localizes to the nucleus and is involved in RNA polymerase II-mediated transcription. It may interact with other transcriptional regulators to modulate gene expression. Expression data suggest a role in brain, breast, and colorectal tissues, with dysregulation observed in several cancers.

Related Products

Product name Cat.No. Species Gene ID
ZNF326 Knockout HEK293 Cell Line EDJ-KQ7481 Human 284695 Details Get a Quote
ZNF326 Knockout A-549 Cell Line EDJ-KQ32709 Human 284695 Details Get a Quote
ZNF326 Knockout HCT 116 Cell Line EDJ-KQ32710 Human 284695 Details Get a Quote
ZNF326 Knockout HeLa Cell Line EDJ-KQ32711 Human 284695 Details Get a Quote
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