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KIF14

kinesin family member 14

HCNC Approved Symbol
KIF14 (HGNC:19181)
Genomic Coordinates
1:200,551,497 - 200,620,751 (1q32.1)
Synonyms
KIAA0042
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Meckel syndrome 12
616258AR
Microcephaly 20, primary, autosomal recessive
617914AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the KIF14 gene.

Frequently observed phenotypes

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

No Results