KIF21A

kinesin family member 21A
OMIM: 608283
PanelMode of inheritanceDetails
3 panels
R-numbers: R83
Signed-off version 5.21
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
arthrogryposis, MONDO:0008779, fetal akinesia
R-numbers: R46
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Congenital fibrosis of the extraocular muscles, Fibrosis of extraocular muscles, congenital, 1 135700, Fibrosis of extraocular muscles, congenital, 3B 135700
R-numbers: R21, R412
Signed-off version 3.122
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arthrogryposis, fetal akinesia