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KIF21B

kinesin family member 21B

HCNC Approved Symbol
KIF21B (HGNC:29442)
Genomic Coordinates
1:200,969,390 - 201,023,714 (1q32.1)
Synonyms
DKFZP434J212, KIAA0449
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.
However, the following publication(s) suggest a possible gene disease association.
View More Disease Info
ContentsPublications
Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity.
PMID:32415109

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the KIF21B gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results