Aliases for SCGB1A1 Gene
External Ids for SCGB1A1 Gene
Previous HGNC Symbols for SCGB1A1 Gene
Previous GeneCards Identifiers for SCGB1A1 Gene
This gene encodes a member of the secretoglobin family of small secreted proteins. The encoded protein has been implicated in numerous functions including anti-inflammation, inhibition of phospholipase A2 and the sequestering of hydrophobic ligands. Defects in this gene are associated with a susceptibility to asthma. [provided by RefSeq, May 2010]
GeneCards Summary for SCGB1A1 Gene
SCGB1A1 (Secretoglobin Family 1A Member 1) is a Protein Coding gene. Diseases associated with SCGB1A1 include Meconium Aspiration Syndrome and Paraquat Lung. Among its related pathways are Prostaglandin Synthesis and Regulation and FOXA1 transcription factor network. GO annotations related to this gene include binding and phospholipase A2 inhibitor activity.
UniProtKB/Swiss-Prot for SCGB1A1 Gene
Binds phosphatidylcholine, phosphatidylinositol, polychlorinated biphenyls (PCB) and weakly progesterone, potent inhibitor of phospholipase A2.