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POU1F1
POU class 1 homeobox 1
gene with protein product
OMIM: 173110
3 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
ORPHA:226307
→
Combined pituitary hormone deficiencies, genetic forms
ORPHA:95494
→
Disease-causing germline mutation(s) (gain of function) in
1
Isolated growth hormone deficiency type II
ORPHA:231679
→
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Редкие заболевания
POU1F1
🧬
POU1F1
POU class 1 homeobox 1
gene with protein product
OMIM: 173110
3 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
2
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
ORPHA:226307
→
Combined pituitary hormone deficiencies, genetic forms
ORPHA:95494
→
Disease-causing germline mutation(s) (gain of function) in
1
Isolated growth hormone deficiency type II
ORPHA:231679
→