KIF21A

kinesin family member 21A
OMIM: 608283, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green KIF21A in Congenital fibrosis of the extraocular muscles Level 2: Ophthalmology Version 2.3 Latest signed off version: v2.0 (30 Apr 2025)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Wessex and West Midlands GLH Literature Phenotypes Fibrosis of extraocular muscles, congenital, 1, OMIM:135700 Fibrosis of extraocular muscles, congenital, 3B, OMIM:135700
Green KIF21A in Arthrogryposis Level 2: Neurology Version 9.24 Latest signed off version: v9.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Literature Phenotypes arthrogryposis, MONDO:0008779 fetal akinesia
Green KIF21A in Fetal anomalies Level 2: Fetal (including NIPD) Version 6.140 Latest signed off version: v6.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Literature Phenotypes Arthrogryposis fetal akinesia
Red KIF21A 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	Not set	Sources Victorian Clinical Genetics Services
Amber KIF21A in Hereditary neuropathy or pain disorder Level 2: Neurology Version 7.36 Latest signed off version: v7.0 (30 Apr 2025)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert list Phenotypes CFEOM agenesis of the corpus callosum peripheral neuropathy, MONDO:0005244 Tags Q4_25_promote_green Q4_25_NHS_review