Gene entry
NYX
nyctalopin
- Chromosome
- X
- Cytoband
- Xp11.4
- Variants (rsID)
- 22
NYX is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.4). Its official name is “nyctalopin”. The reference table lists 22 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs62637035Likely pathogenicsingle nucleotide variant
- rs104894911Pathogenicsingle nucleotide variantCongenital stationary night blindness 1A
- rs62637037Uncertain significancesingle nucleotide variantCongenital stationary night blindness 1A
- rs62637024Not classifiedsingle nucleotide variant
- rs62637028Not classifiedsingle nucleotide variant
- rs62637030Not classifiedsingle nucleotide variant
- rs62637032Not classifiedsingle nucleotide variant
- rs62637033Not classifiedsingle nucleotide variant
- rs62637034Not classifiedsingle nucleotide variant
- rs62637036Not classifiedsingle nucleotide variant
- rs62637038Not classifiedsingle nucleotide variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.