Table 2.
Phenotype of CCC mutations.
| CCC | Location | Mutation | Species | Neurological effect | Ref. |
|---|---|---|---|---|---|
| KCC1 | Ubiquitous | Knockout | Mouse | None seen | [92] |
| KCC2 | Brain | KCC2a and KCC2b knockout | Mouse | Death at birth | [93] |
| Brain | KCC2b knockout | Mouse | Seizures, low weight, early mortality | [94] | |
| Brain | Hypomorph | Mouse | Increased seizure susceptibility and anxiety | [95] | |
| Brain | Heterozygote | Mouse | Hyperexcitability | [96] | |
| KCC3 | Ubiquitous | KCC3a-c knockout | Human, mouse | Peripheral neuropathy; seizures have been reported | [97–100] |
| KCC4 | Kidney, heart, lungs, liver | Knockout | Mouse | Deafness | [101] |
| NKCC1 | Ubiquitous | NKCC1a knockout | Mouse | Deafness, circling behavior | [102] |
| Ubiquitous | NKCC1a and NKCC1b knockout | Mouse | Deafness, circling behavior, growth retardation, defective spermatogenesis, increased threshold to thermal stimulation | [103, 104] | |
| NKCC2 | Kidney | Knockout | Human | Bartter's syndrome | [105] |