Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b

Summary

Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b is a protein^[1].

Key Facts

• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's instance of is recorded as protein^[2].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's UniProt protein ID is recorded as A0A024QZQ2^[3].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's part of is recorded as saposin, chordata^[4].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's part of is recorded as saposin-like^[5].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's part of is recorded as saposin B type domain, protein family^[6].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's part of is recorded as Saposin B type, region 2, protein family^[7].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's part of is recorded as Saposin A-type domain, protein family^[8].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's part of is recorded as Saposin-like type B, region 1, protein family^[9].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's has part is recorded as saposin-like type B, region 1^[10].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's has part is recorded as saposin A-type domain^[11].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's has part is recorded as saposin B type, region 2^[12].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's has part is recorded as saposin B type domain^[13].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's RefSeq protein ID is recorded as NP_002769.1^[14].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's molecular function is recorded as G protein-coupled receptor binding^[15].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's cell component is recorded as lysosome^[16].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's cell component is recorded as intracellular membrane-bounded organelle^[17].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's cell component is recorded as cytoplasm^[18].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's cell component is recorded as extracellular region^[19].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's biological process is recorded as cellular response to organic substance^[20].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's biological process is recorded as regulation of lipid metabolic process^[21].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's biological process is recorded as prostate gland growth^[22].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's biological process is recorded as negative regulation of hydrogen peroxide-induced cell death^[23].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's biological process is recorded as developmental growth^[24].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's biological process is recorded as adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway^[25].
• Prosaposin (Variant Gaucher disease and variant metachromatic leukodystrophy), isoform CRA_b's biological process is recorded as regulation of MAPK cascade^[26].