Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Cis-regulatory Sequences02:02

Cis-regulatory Sequences

Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
Cis-regulatory Sequences02:02

Cis-regulatory Sequences

Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
Genetic Screens02:46

Genetic Screens

Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing  genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which result in visible changes...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Development of a Prediction Model for Severe Pediatric <i>Mycoplasma pneumoniae</i> Pneumonia: A Single-Center Retrospective Study.

Infection and drug resistance·2026
Same author

Single-cell RNA sequencing unraveled immune-related expression heterogeneity and lymphoid cell development dysregulation in childhood asthma.

Frontiers in immunology·2026
Same author

Patients Suffering From Post-COVID-19 Syndrome Feature Enhanced Antibody Reactivity Towards Specific Linear Epitopes Within EBV EBNA1.

Scandinavian journal of immunology·2026
Same author

Accelerated biological aging based on DNA methylation clocks is a predictor of stroke occurrence: a systematic review and meta-analysis.

Frontiers in neurology·2025
Same author

Osseointegration of threaded acetabular cups - radiological and histological evaluation after total hip arthroplasty.

International orthopaedics·2025
Same author

Single cell sequencing technology reveals the correlation between B lymphocytes and vascular inflammatory symptoms of Kawasaki disease.

Translational pediatrics·2025

Related Experiment Video

Updated: Jun 28, 2026

Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains
11:24

Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains

Published on: March 25, 2015

SysZNF: the C2H2 zinc finger gene database.

Guohui Ding1, Peter Lorenz, Michael Kreutzer

  • 1Bioinformatics Center, Key Lab of Systems Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai 200031, P. R. China.

Nucleic Acids Research
|November 1, 2008
PubMed
Summary

SysZNF is a new database cataloging human and mouse C2H2 zinc finger (C2H2-ZNF) genes. This resource aids genotype-phenotype comparisons and understanding C2H2-ZNF gene evolution.

More Related Videos

Genome Editing with CompoZr Custom Zinc Finger Nucleases (ZFNs)
09:11

Genome Editing with CompoZr Custom Zinc Finger Nucleases (ZFNs)

Published on: June 14, 2012

Embryo Microinjection and Electroporation in the Chordate Ciona intestinalis
09:38

Embryo Microinjection and Electroporation in the Chordate Ciona intestinalis

Published on: October 16, 2016

Related Experiment Videos

Last Updated: Jun 28, 2026

Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains
11:24

Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains

Published on: March 25, 2015

Genome Editing with CompoZr Custom Zinc Finger Nucleases (ZFNs)
09:11

Genome Editing with CompoZr Custom Zinc Finger Nucleases (ZFNs)

Published on: June 14, 2012

Embryo Microinjection and Electroporation in the Chordate Ciona intestinalis
09:38

Embryo Microinjection and Electroporation in the Chordate Ciona intestinalis

Published on: October 16, 2016

Area of Science:

  • Genomics
  • Bioinformatics
  • Evolutionary Biology

Background:

  • C2H2 zinc finger (C2H2-ZNF) genes represent a vast and intricate gene super-family in metazoan genomes.
  • Hundreds of C2H2-ZNF genes exist in human and mouse genomes, necessitating computational tools for comprehensive study.

Purpose of the Study:

  • To systematically collect and organize C2H2-ZNF gene data from human and mouse genomes.
  • To create a centralized database (SysZNF) for genotype-phenotype comparisons and evolutionary analysis of C2H2-ZNF genes.

Main Methods:

  • Systematic collection of all C2H2-ZNF genes from human and mouse genomes.
  • Construction of the SysZNF database, integrating gene location, models, expression data, protein domains, homologs, and literature links.
  • Implementation of search functionalities (text and sequence) and data download options.

Main Results:

  • The SysZNF database provides comprehensive data for each C2H2-ZNF gene, including physical location, transcript forms, expression probes, protein domains, and homologous genes.
  • The database highlights the clustered organization of C2H2-ZNF genes and facilitates synteny analysis between human and mouse.
  • Integrated tools within SysZNF, such as graphical views and sequence retrieval, support an integrative approach to C2H2-ZNF gene research.

Conclusions:

  • SysZNF serves as a valuable computational resource for researchers studying C2H2-ZNF genes.
  • The database supports genotype-phenotype comparisons and advances the understanding of C2H2-ZNF gene evolution across species.