1. Genes and Genomic Entities
  2. KIF21B

KIF21B

kinesin family member 21B
OMIM: 608322, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber KIF21B in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • NHS GMS
  • Expert Review Amber
Phenotypes
  • Global developmental delay
  • Neurodevelopmental disorder, MONDO:0700092
  • Intellectual disability
  • Abnormality of brain morphology
  • Microcephaly
Green KIF21B in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Global developmental delay
    • Intellectual disability
    • Abnormality of brain morphology
    • Microcephaly
    Tags
    • gene-checked