| ID | Sequence | Length | GC content |
|---|---|---|---|
| AUACAGAAGGCGCUUGGCUCAGGGUACACAGGGCAAGAAGCCUCGGAUC… | 2416 nt | 0.4077 | |
| AAUCUGCAGCAGAGAUUUACCCGAGCGUGUUGCGGCAGCGGCUGGGCUU… | 2658 nt | 0.4176 | |
| AAUCUGCAGCAGAGAUUUACCCGAGCGUGUUGCGGCAGCGGCUGGGCUU… | 2212 nt | 0.3883 | |
| AAUCUGCAGCAGAGAUUUACCCGAGCGUGUUGCGGCAGCGGCUGGGCUU… | 2424 nt | 0.4006 | |
| AAUCUGCAGCAGAGAUUUACCCGAGCGUGUUGCGGCAGCGGCUGGGCUU… | 2428 nt | 0.4012 |
This gene is a member of the visinin/recoverin subfamily of neuronal calcium sensor proteins. The encoded protein is strongly expressed in granule cells of the cerebellum where it associates with membranes in a calcium-dependent manner and modulates intracellular signaling pathways of the central nervous system by directly or indirectly regulating the activity of adenylyl cyclase. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]
A study in mice demonstrated that VSNL1 was significantly up-regulated across seven brain regions in ethanol-naïve High Drinking in the Dark (HDID-1) mice compared to control mice, with a fold change range of 1.23–1.49, identifying it as a differentially expressed gene associated with a genetic predisposition for binge drinking [Ferguson et al. DOI:10.1007/S12035-018-1252-0].