KIF3B - Gene browser | 3billion

KIF3B

KIF3B

kinesin family member 3B

HCNC Approved Symbol: KIF3B (HGNC:6320)
Genomic Coordinates: 20:32,277,651 - 32,335,011 (20q11.21)
Synonyms: KIAA0359, FLA8, KLP-11
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the KIF3B gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Progressive visual loss: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Retinitis pigmentosa: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Rod-cone dystrophy: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Uveitis: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)

Last updated: 2024-06-30

KIF3B - Gene browser | 3billion