KIF21B

kinesin family member 21B
OMIM: 608322, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green KIF21B in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Global developmental delay
  • Intellectual disability
  • Abnormality of brain morphology
  • Microcephaly

Green KIF21B in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Global developmental delay
  • Intellectual disability
  • Abnormality of brain morphology
  • Microcephaly

Green KIF21B in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

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

Green KIF21B in Fetal anomalies


Version 1.255

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