1. Genes and Genomic Entities
  2. KIF3B

KIF3B

kinesin family member 3B
OMIM: 603754, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red KIF3B in DDG2P


Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • KIF3B-related ciliopathy
    Amber KIF3B in Retinal disorders

    Level 3: Posterior segment abnormalities
    Level 2: Ophthalmological disorders
    Version 5.4
    Latest signed off version: v5.0 (1 May 2024)

    		review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Literature
    • Expert list
    Phenotypes
    • hepatic fibrosis
    • Retinitis pigmentosa 89, OMIM:618955, MONDO:0030071
    • postaxial polydactyly
    Tags
    • watchlist
    Amber KIF3B in Ophthalmological ciliopathies


    Version 4.1
    Latest signed off version: v4.0 (1 May 2024)

    Component of the following Super Panels:

  • Paediatric disorders
  • Rare multisystem ciliopathy Super panel

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • hepatic fibrosis
    • Retinitis pigmentosa 89, OMIM:618955, MONDO:0030071
    • postaxial polydactyly
    Tags
    • watchlist