2yad: Difference between revisions
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== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/PSPC_HUMAN PSPC_HUMAN] Interstitial lung disease due to SP-C deficiency | [https://www.uniprot.org/uniprot/PSPC_HUMAN PSPC_HUMAN] Infant acute respiratory distress syndrome;Interstitial lung disease due to SP-C deficiency;Chronic respiratory distress with surfactant metabolism deficiency;Idiopathic pulmonary fibrosis. The disease is caused by variants affecting the gene represented in this entry. | ||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/PSPC_HUMAN PSPC_HUMAN] Pulmonary surfactant associated proteins promote alveolar stability by lowering the surface tension at the air-liquid interface in the peripheral air spaces. | [https://www.uniprot.org/uniprot/PSPC_HUMAN PSPC_HUMAN] Pulmonary surfactant associated proteins promote alveolar stability by lowering the surface tension at the air-liquid interface in the peripheral air spaces. | ||