Cystic fibrosis is an autosomal recessive disorder caused by a mutation to the CFTR gene on chromosome 7, producing thick, sticky mucus that clogs airways and digestive ducts; heterozygous carriers do not develop symptoms.
La fibrosis quística es un trastorno autosómico recesivo causado por una mutación en el gen CFTR del cromosoma 7, que produce moco espeso y pegajoso, obstruyendo vías respiratorias y conductos digestivos; los portadores heterocigotos no desarrollan síntomas.
Original | CFTR gene on chromosome 7 produce mucus which is unusually thick and sticky clogs the airways and secretory ducts of the digestive system, leading to respiratory failure and pancreatic cysts Heterozygous carriers who possess one normal allele will not develop disease symptoms |
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Title | Cystic fibrosis is an autosomal recessive disorder caused by a mutation to the ... Individuals with cystic fibrosis will ... which ... |
Settings | 1,1,0 | n,n,n,n |
Text1 | CFTR gene on chromosome 7 ... ... ... |
Text2 | CFTR gene on chromosome 7 produce mucus which is unusually thick and sticky ... ... |
Text3 | ... produce mucus which is unusually thick and sticky clogs the airways and secretory ducts of the digestive system, leading to respiratory failure and pancreatic cysts ... |
Text4 | ... ... clogs the airways and secretory ducts of the digestive system, leading to respiratory failure and pancreatic cysts Heterozygous carriers who possess one normal allele will not develop disease symptoms |
Full | CFTR gene on chromosome 7 produce mucus which is unusually thick and sticky clogs the airways and secretory ducts of the digestive system, leading to respiratory failure and pancreatic cysts Heterozygous carriers who possess one normal allele will not develop disease symptoms |
Tags: 3_4_inheritance, cystic_fibrosis
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