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Predicted to react with Mouse and Rat samples.
This gene encodes a protein involved intracellular vesicle and organelle transport, especially in the hair cell of the inner ear. Mutations in this gene have been found in patients with non-syndromic autosomal dominant and recessive hearing loss.
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: myosin VI; myosin-VI; Protein twist; Snell's waltzer; tailchaser; Unconventional myosin-6; Unconventional myosin-VI
基因别名: BC029719; DFNA22; DFNB37; KIAA0389; MYO6; RGD1560646; Sv; Tlc
UniProt ID: (Human) Q9UEG2, (Mouse) Q64331
Entrez Gene ID: (Human) 4646, (Mouse) 17920, (Rat) 315840