1. Genes and Genomic Entities
  2. KIF26A

KIF26A

kinesin family member 26A
OMIM: 613231, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels
Amber KIF26A in Hydrocephalus


Level 2: Neurology
Version 5.8
Latest signed off version: v5.0 (7 Aug 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Other
Phenotypes
  • Cortical dysplasia, complex, with other brain malformations 11, OMIM:620156
  • cortical dysplasia, complex, with other brain malformations 11 MONDO:0859332
Tags
  • Q4_25_promote_green
Amber KIF26A in Malformations of cortical development


Level 2: Neurology
Version 7.30
Latest signed off version: v7.0 (30 Oct 2024)

Component of the following Super Panels:

  • Cerebral malformation

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Other
    Phenotypes
    • Cortical dysplasia, complex, with other brain malformations 11, OMIM:620156
    • cortical dysplasia, complex, with other brain malformations 11 MONDO:0859332
    Tags
    • Q4_25_promote_green
    Green KIF26A in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 6.138
    Latest signed off version: v6.0 (30 Apr 2025)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Cortical dysplasia, complex, with other brain malformations 11, OMIM:620156
    Amber KIF26A in Intellectual disability


    Level 2: Developmental disorders
    Version 9.279
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Other
    Phenotypes
    • Cortical dysplasia, complex, with other brain malformations 11, OMIM:620156
    • cortical dysplasia, complex, with other brain malformations 11 MONDO:0859332
    Amber KIF26A in Paediatric pseudo-obstruction syndrome


    Level 2: Gastrohepatology
    Version 2.5
    Latest signed off version: v2.0 (30 Apr 2025)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Cortical dysplasia, complex, with other brain malformations 11, OMIM:620156
    • cortical dysplasia, complex, with other brain malformations 11 MONDO:0859332
    Tags
    • Q4_25_promote_green
    • Q4_25_NHS_review