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SLC26A2

solute carrier family 26 member 2

gene with protein productOMIM: 6067184 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3
Atelosteogenesis type IIORPHA:56304
→
Achondrogenesis type 1BORPHA:93298
→
Multiple epiphyseal dysplasia type 4ORPHA:93307
→
Disease-causing germline mutation(s) (loss of function) in1
Diastrophic dysplasiaORPHA:628
→
Данные: Orphadata (CC-BY-4.0)