Gene

Zfp469

Species
Mus musculus
Symbol
Zfp469
Name
zinc finger protein 469
Synonyms
  • gene model 22, (NCBI)
  • Gm22
Biotype
protein coding gene
Automated Description
Acts upstream of or within several processes, including extracellular matrix organization; fibroblast proliferation; and substantia propria of cornea development. Is expressed in several structures, including craniocervical region bone; sensory organ; skeleton; tarsus; and urinary system. Used to study brittle cornea syndrome 1. Human ortholog(s) of this gene implicated in brittle cornea syndrome 1. Orthologous to human ZNF469 (zinc finger protein 469).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR21465
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
122.986M122.988M122.990M122.992M122.994M122.996M122.998M

Sequence Details

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Expression

Primary Sources
Other Sources
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions