| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGCUCCGCUCUGCCUCCGGCUCUGCGCUCACCUGCUGCCUAGUGUUCCC… | 2469 nt | 0.5597 | |
| AGCUCCGCUCUGCCUCCGGCUCUGCGCUCACCUGCUGCCUAGUGUUCCC… | 2424 nt | 0.5590 | |
| AGCUCCGCUCUGCCUCCGGCUCUGCGCUCACCUGCUGCCUAGUGUUCCC… | 2370 nt | 0.5549 | |
| AGCUCCGCUCUGCCUCCGGCUCUGCGCUCACCUGCUGCCUAGUGUUCCC… | 2295 nt | 0.5529 | |
| GGAGCUUAGACGCCGAGCUCGCCGCCAAACCAUGAACCGAUGCCCCCGC… | 2088 nt | 0.5350 | |
| AGCUCCGCUCUGCCUCCGGCUCUGCGCUCACCUGCUGCCUAGUGUUCCC… | 2274 nt | 0.5519 | |
| AGCUCCGCUCUGCCUCCGGCUCUGCGCUCACCUGCUGCCUAGUGUUCCC… | 787 nt | 0.5934 |
This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins (KCNIPs), which belongs to the recoverin branch of the EF-hand superfamily. Members of the KCNIP family are small calcium binding proteins. They all have EF-hand-like domains, and differ from each other in the N-terminus. They are integral subunit components of native Kv4 channel complexes. They may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified from this gene. [provided by RefSeq, Jul 2008]
A study in mice demonstrated that the KCNIP2 was identified in a complete alternative splicing list from a heart-specific double knockout model, which recapitulated myotonic dystrophy cardiac pathogenesis and sudden death, with findings compatible with another mouse model [Lee et al. DOI:10.1093/hmg/ddac108]. A study in rats demonstrated that in a model of acute right heart failure induced by pulmonary artery banding, the KCNIP2 was identified as a protein with more interactive evidence in the right ventricle versus left ventricle protein-protein interaction network [Cao et al. DOI:10.1177/2045894019879396].