KIF11 - Gene browser

KIF11

kinesin family member 11

HCNC Approved Symbol: KIF11 (HGNC:6388)
Genomic Coordinates: 10:92,593,130 - 92,655,395 (10q23.33)
Synonyms: Eg5, HKSP, TRIP5, KNSL1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

17Patients

In total, 17 patients were diagnosed with a variant in the KIF11 gene.

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

017
Patient count

Microcephaly: 9 (52.9%)
Patient Count: 9 (52.9%)
% of total patients presenting each phenotype is shown in parentheses.
9 (52.9%)
Global developmental delay: 3 (17.6%)
Patient Count: 3 (17.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (17.6%)
Intrauterine growth retardation: 3 (17.6%)
Patient Count: 3 (17.6%)
% of total patients presenting each phenotype is shown in parentheses.
3 (17.6%)
Nystagmus: 2 (11.8%)
Patient Count: 2 (11.8%)
% of total patients presenting each phenotype is shown in parentheses.
2 (11.8%)
Delayed fine motor development: 2 (11.8%)
Patient Count: 2 (11.8%)
% of total patients presenting each phenotype is shown in parentheses.
2 (11.8%)