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Proteintech
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Immunogen sequence: RYINKALECF DSSVFGAIYY VVFTTLVLLA SAILFREWSN VGLVDFLGMA CGFTTVSVGI VLIQVFKEFN FNLGEMNKSN MKTD
This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6.
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: Magnesium transporter NIPA1; non imprinted in Prader-Willi/Angelman syndrome 1 homolog; non-imprinted in Prader-Willi/Angelman syndrome 1; Non-imprinted in Prader-Willi/Angelman syndrome region protein 1; Non-imprinted in Prader-Willi/Angelman syndrome region protein 1 homolog; spastic paraplegia 6 (autosomal dominant); spastic paraplegia 6 homolog; Spastic paraplegia 6 protein
基因别名: 1110027G09Rik; A830014A18Rik; FSP3; NIPA1; SPG6
UniProt ID: (Human) Q7RTP0, (Mouse) Q8BHK1
Entrez Gene ID: (Human) 123606, (Mouse) 233280, (Rat) 308668