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The protein encoded by this gene is a Rho-like GTPase that switches between the active state and inactive state to regulate CDC42 and other genes. Defects in this gene are a cause of startle disease with epilepsy, also known as hyperekplexia with epilepsy. Three transcript variants encoding different isoforms have been found for this gene.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Collybistin; Rac/Cdc42 guanine nucleotide exchange factor 9; Rho guanine nucleotide exchange factor 9
基因别名: 9630036L12Rik; A230067K14; Arhgef9; Kiaa0424; mKIAA0424
UniProt ID: (Mouse) Q3UTH8
Entrez Gene ID: (Mouse) 236915