Gene entry
KIFBP
kinesin family binding protein
- Chromosome
- 10
- Cytoband
- 10q22.1
- Variants (rsID)
- 13
KIFBP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q22.1). Its official name is “kinesin family binding protein”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs41279644Benignsingle nucleotide variantGoldberg-Shprintzen megacolon syndrome
- rs62625033Benignsingle nucleotide variantGoldberg-Shprintzen megacolon syndrome
- rs730882150Pathogenicsingle nucleotide variantGoldberg-Shprintzen megacolon syndrome
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.
