KIF23 Chromosome 15

Kinesin family member 23
13 variants 13 Health Risk

Upload your DNA to see your personal genotypes for variants in KIF23.

What This Gene Does
The protein encoded by this gene is a member of kinesin-like protein family. This family includes microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. This protein has been shown to cross-bridge antiparallel microtubules and drive microtubule movement in vitro. Alternate splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Gene Info
Gene Group
Kinesins
Locus Type
gene with protein product
Location
15q23
Ensembl
ENSG00000137807
Associated Conditions (6)
KIF23-related disorder
Malignant tumor of urinary bladder
Ovarian serous cystadenocarcinoma
Congenital dyserythropoietic anemia
type III
Microcephaly
Key Variants
All Variants (13)
RSID Category Clinical Significance Conditions
RS137922672 Health Risk Conflicting classifications of pathogenicity KIF23-related disorder, KIF23-related disorder
RS143219911 Health Risk Conflicting classifications of pathogenicity
RS148511930 Health Risk Conflicting classifications of pathogenicity
RS150307169 Health Risk Conflicting classifications of pathogenicity KIF23-related disorder, KIF23-related disorder
RS199679829 Health Risk Conflicting classifications of pathogenicity Malignant tumor of urinary bladder, Malignant tumor of urinary bladder
RS372828681 Health Risk Conflicting classifications of pathogenicity
RS375380237 Health Risk Conflicting classifications of pathogenicity
RS543990042 Health Risk Conflicting classifications of pathogenicity Ovarian serous cystadenocarcinoma, Ovarian serous cystadenocarcinoma
RS560614661 Health Risk Conflicting classifications of pathogenicity
RS748182171 Health Risk Conflicting classifications of pathogenicity
RS2140422904 Health Risk Likely pathogenic Congenital dyserythropoietic anemia, type III, Congenital dyserythropoietic anemia
RS748016594 Health Risk Likely pathogenic Microcephaly, Microcephaly
RS2140424959 Health Risk Pathogenic Congenital dyserythropoietic anemia, type III, Congenital dyserythropoietic anemia
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