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中文小鼠
Cln3 - ceroid lipofuscinosis, neuronal 3, juvenile (Batten, Spielmeyer-Vogt disease)
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这个基因编码一种叫做battenin的跨膜蛋白，参与溶酶体功能。这个基因以及其他神经鞘脂沉积症基因的突变，导致了许多神经退行性疾病，统称为神经鞘脂沉积症，最常见的是少年神经鞘脂沉积症（巴滕病）。可变剪接产生了多种转录子变异体。[RefSeq, 2016年8月提供]
Basic Information
NCBI
Transcripts
Exons
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MW (kDa)
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Cln3 Genetics information (-)
GRCm39
Sequence Homology
Transcripts & Proteins
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CDS(bp)
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* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
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Cell-specific RNA expression
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