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Protein Coding Gene : Kalrn kalirin, RhoGEF kinase

Primary Identifier  MGI:2685385 Organism  mouse, laboratory
Chromosome  16 NCBI Gene Number  545156
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable enzyme binding activity and guanyl-nucleotide exchange factor activity. Acts upstream of or within several processes, including learning or memory; maternal behavior; and maternal process involved in parturition. Predicted to be located in several cellular components, including neuronal cell body; nucleoplasm; and perinuclear region of cytoplasm. Predicted to be active in several cellular components, including glutamatergic synapse; postsynaptic density; and presynapse. Predicted to be extrinsic component of membrane. Is expressed in dorsal root ganglion and spinal cord. Human ortholog(s) of this gene implicated in cerebral atherosclerosis; cerebral infarction; and coronary artery disease. Orthologous to human KALRN (kalirin RhoGEF kinase).
PHENOTYPE: Mice homozygous for a knock-out allele specific for isoform 7 exhibit decreased anxiety-related behavior, contextual conditioning, and synapse formation. Mice homozygous for another knock-out allele exhibit impaired AMPA-mediated synaptic currents and abnormal behavior. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 2210407G14 gene,
  • MGI:1919628,
  • LOC224126,
  • MGI:2443174,
  • E530005C20Rik,
  • RIKEN cDNA E530005C20 gene,
  • expressed sequence AV235988,
  • Kalrn,
  • huntingtin-associated protein interacting protein (duo),
  • Hapip,
  • 2210407G14Rik,
  • gene model 539, (NCBI),
  • AV235988,
  • MGI:2146601,
  • kalirin, RhoGEF kinase,
  • Gm539

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