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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.