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Adding 0.2 mL of distilled water will yield a concentration of 500 µg/mL.
CHCHD10 encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. Mutations in this gene cause frontotemporal dementia and/or amyotrophic lateral sclerosis-2. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7 and 19.
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: Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial; Nur77 downstream gene 2; Nur77 downstream protein 2; Protein N27C7-4
基因别名: 1620401E04Rik; AI267078; C22orf16; CHCHD10; FTDALS2; IMMD; N27C7-4; Ndg2; SMAJ
UniProt ID: (Human) Q8WYQ3
Entrez Gene ID: (Human) 400916, (Mouse) 103172, (Rat) 361824