Query author contributions in Reactome
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Details on Person Five members of the NCKX (SLC24) family are all able to exch...
| Class:Id | Summation:5625843 |
|---|---|
| _displayName | Five members of the NCKX (SLC24) family are all able to exch... |
| _timestamp | 2014-10-09 08:58:30 |
| created | [InstanceEdit:5625839] Jassal, Bijay, 2014-10-08 |
| modified | [InstanceEdit:5626263] Jassal, Bijay, 2014-10-09 |
| text | Five members of the NCKX (SLC24) family are all able to exchange one Ca2+ and one K+ for four Na+. SLC24A1 encodes an exchanger protein NCKX1 which is the most extensively studied member and is highly expressed in the eye. The light-induced lowering of calcium by efflux via this protein plays a key role in the process of light adaptation (Schnetkamp 2013). Defects in SLC24A1 can cause congenital stationary night blindness 1D (CSNB1D), an autosomal recessive, non-progressive retinal disorder characterised by impaired night vision and characterised by a Riggs-type of electroretinogram (Riazuddin et al. 2010). |
| (summation) | [Pathway:5619077] Defective SLC24A1 causes congenital stationary night blindness 1D (CSNB1D) [Homo sapiens] |
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No pathways have been reviewed or authored by Five members of the NCKX (SLC24) family are all able to exch... (5625843)
