← Назад
🧬
KIF21A
kinesin family member 21A
gene with protein product
OMIM: 608283
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Fetal akinesia deformation sequence
ORPHA:994
→
Герминативная мутация (причина)
1
Congenital fibrosis of extraocular muscles
ORPHA:45358
→
Home
Calc.
Tools
Sign in
MEDLIB
Home
Tools
Pricing
Sign in
Language
ҚАЗ
EN
DE
RU
Главная
Инструменты
Редкие заболевания
KIF21A
🧬
KIF21A
kinesin family member 21A
gene with protein product
OMIM: 608283
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Fetal akinesia deformation sequence
ORPHA:994
→
Герминативная мутация (причина)
1
Congenital fibrosis of extraocular muscles
ORPHA:45358
→