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Positive Samples: 293T, Mouse kidney; Cellular Location: Cell membrane, Membrane, Multi-pass membrane protein
Immunogen sequence: MAAATRRVFH LQPCENSPTM SQNGYFEDSS YYKCDTDDTF EAREEILGDE AFDTANSSIV SGESIRFFVN VNLEMQATNT ENEATSGGCV LLHTSRKYLK LKNFKEEIRA HRDLDGFLAQ ASIVLNETAT SLDNVLRTML RRFARDPDNN EPNCNLDLLM AMLFTDAGAP MRGKVHLLSD
This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described.
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: bicarbonate transporter related protein 1; bicarbonate transporter-related protein 1; CDPD; MGC126418; MGC126419; NaBC1; OTTHUMP00000030097; sodium bicarbonate transporter-like protein 11; Sodium borate cotransporter 1; sodium-coupled borate cotransporter 1; Solute carrier family 4 member 11; solute carrier family 4, sodium bicarbonate transporter-like, member 11; solute carrier family 4, sodium borate transporter, member 11
基因别名: AI503023; BTR1; CDPD1; CHED; CHED2; dJ794I6.2; NABC1; SLC4A11
UniProt ID: (Human) Q8NBS3, (Mouse) A2AJN7
Entrez Gene ID: (Human) 83959, (Mouse) 269356