CIT

Filters:

Results for "CIT": 1 gene, 8 gene sets

Name
CIT Gene citron rho-interacting serine/threonine kinase This gene encodes a serine/threonine-protein kinase that functions in cell division. Together with the kinesin KIF14, this protein localizes to the central spindle and midbody, and functions to promote efficient cytokinesis. This protein is involved in central nervous system development. Polymorphisms in this gene are associated with bipolar disorder and risk for schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]
cit Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cit in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
CIT Gene Set From KEA Substrates of Kinases substrates of the kinase CIT from the curated KEA Substrates of Kinases dataset.
CIT Gene Set From Pathway Commons Protein-Protein Interactions interacting proteins for CIT from the Pathway Commons Protein-Protein Interactions dataset.
CIT Gene Set From PhosphoSitePlus Substrates of Kinases substrates of the kinase CIT from the curated PhosphoSitePlus Substrates of Kinases dataset.
CIT Gene Set From LINCS L1000 CMAP CRISPR Knockout Consensus Signatures genes differentially expressed following the CIT gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset.
CIT Gene Set From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the CIT gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.
RHO GTPases activate CIT Gene Set From Reactome Pathways 2024 proteins participating in the RHO GTPases activate CIT pathway from the Reactome Pathways 2024 dataset.
Executive inhibition (Stroop WIT and CIT) in attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Executive inhibition (Stroop WIT and CIT) in attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.