Gene entry
NDP
norrin cystine knot growth factor NDP
- Chromosome
- X
- Cytoband
- Xp11.3
- Variants (rsID)
- 18
NDP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.3). Its official name is “norrin cystine knot growth factor NDP”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs5952410Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs3747350Likely benignsingle nucleotide variant
- rs104894868Pathogenicsingle nucleotide variantAtrophia bulborum hereditaria
- rs104894869Pathogenicsingle nucleotide variantAtrophia bulborum hereditaria
- rs104894872Pathogenicsingle nucleotide variantAtrophia bulborum hereditaria
- rs104894874Pathogenicsingle nucleotide variantExudative vitreoretinopathy, X-linked
- rs104894877Pathogenicsingle nucleotide variantAtrophia bulborum hereditaria
- rs104894878Pathogenicsingle nucleotide variantExudative vitreoretinopathy 2, X-linked
- rs137852221Pathogenicsingle nucleotide variantAtrophia bulborum hereditaria
- rs104894867Uncertain significancesingle nucleotide variantAtrophia bulborum hereditaria
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.