Aliases for ZNF195 Gene
External Ids for ZNF195 Gene
Previous GeneCards Identifiers for ZNF195 Gene
This gene encodes a protein belonging to the Krueppel C2H2-type zinc-finger protein family. These family members are transcription factors that are implicated in a variety of cellular processes. This gene is located near the centromeric border of chromosome 11p15.5, next to an imprinted domain that is associated with maternal-specific loss of heterozygosity in Wilms' tumors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]
GeneCards Summary for ZNF195 Gene
ZNF195 (Zinc Finger Protein 195) is a Protein Coding gene. Diseases associated with ZNF195 include Wilson-Turner X-Linked Mental Retardation Syndrome. Among its related pathways are Herpes simplex virus 1 infection and Gene Expression. Gene Ontology (GO) annotations related to this gene include nucleic acid binding. An important paralog of this gene is ZNF43.
UniProtKB/Swiss-Prot for ZNF195 Gene
May be involved in transcriptional regulation.