| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| Y44E3A.6 | car-1 | Y44E3A.6b.1 | Y18D10A.17.1 | FHA domain-containing protein. | Cytokinesis, Apoptosis, RNA-associated. | 0.585 |
| Y44E3A.6 | cgh-1 | Y44E3A.6b.1 | C07H6.5.1 | FHA domain-containing protein. | ATP-dependent RNA helicase cgh-1; Probable RNA helicase required for oocyte and sperm function. Also required to prevent the physiological germline apoptosis mechanism killing essentially all developing oocytes. Belongs to the DEAD box helicase family. DDX6/DHH1 subfamily. | 0.967 |
| Y44E3A.6 | dcap-2 | Y44E3A.6b.1 | F52G2.1b.1 | FHA domain-containing protein. | mRNA-decapping enzyme 2; RNA-decapping enzyme although it does not bind cap. May contribute to gene regulation in multiple RNA pathways including monomethylguanosine- and trimethylguanosine-capped RNAs. Belongs to the Nudix hydrolase family. DCP2 subfamily. | 0.989 |
| Y44E3A.6 | edc-3 | Y44E3A.6b.1 | R05D11.8.1 | FHA domain-containing protein. | DFDF domain-containing protein. | 0.801 |
| Y44E3A.6 | ifet-1 | Y44E3A.6b.1 | F56F3.1.1 | FHA domain-containing protein. | Translational repressor ifet-1; Involved in translational repression of multiple mRNAs in the distal gonad. Recruited to the 3' untranslated region (UTR) of zif-1 by oma-1 and is required for translational repression of zif-1. May also be involved in translational repression of mei-1 through recruitment to the mei-1 3' UTR by oma-1. Required for oogenesis but not spermatogenesis, for P granule formation and for the localization of car-1 and cgh-1 to P granules. Required for normal spindle orientation in early embryos. | 0.461 |
| car-1 | Y44E3A.6 | Y18D10A.17.1 | Y44E3A.6b.1 | Cytokinesis, Apoptosis, RNA-associated. | FHA domain-containing protein. | 0.585 |
| car-1 | cgh-1 | Y18D10A.17.1 | C07H6.5.1 | Cytokinesis, Apoptosis, RNA-associated. | ATP-dependent RNA helicase cgh-1; Probable RNA helicase required for oocyte and sperm function. Also required to prevent the physiological germline apoptosis mechanism killing essentially all developing oocytes. Belongs to the DEAD box helicase family. DDX6/DHH1 subfamily. | 0.999 |
| car-1 | dcap-2 | Y18D10A.17.1 | F52G2.1b.1 | Cytokinesis, Apoptosis, RNA-associated. | mRNA-decapping enzyme 2; RNA-decapping enzyme although it does not bind cap. May contribute to gene regulation in multiple RNA pathways including monomethylguanosine- and trimethylguanosine-capped RNAs. Belongs to the Nudix hydrolase family. DCP2 subfamily. | 0.982 |
| car-1 | edc-3 | Y18D10A.17.1 | R05D11.8.1 | Cytokinesis, Apoptosis, RNA-associated. | DFDF domain-containing protein. | 0.496 |
| car-1 | ifet-1 | Y18D10A.17.1 | F56F3.1.1 | Cytokinesis, Apoptosis, RNA-associated. | Translational repressor ifet-1; Involved in translational repression of multiple mRNAs in the distal gonad. Recruited to the 3' untranslated region (UTR) of zif-1 by oma-1 and is required for translational repression of zif-1. May also be involved in translational repression of mei-1 through recruitment to the mei-1 3' UTR by oma-1. Required for oogenesis but not spermatogenesis, for P granule formation and for the localization of car-1 and cgh-1 to P granules. Required for normal spindle orientation in early embryos. | 0.998 |
| cgh-1 | Y44E3A.6 | C07H6.5.1 | Y44E3A.6b.1 | ATP-dependent RNA helicase cgh-1; Probable RNA helicase required for oocyte and sperm function. Also required to prevent the physiological germline apoptosis mechanism killing essentially all developing oocytes. Belongs to the DEAD box helicase family. DDX6/DHH1 subfamily. | FHA domain-containing protein. | 0.967 |
| cgh-1 | car-1 | C07H6.5.1 | Y18D10A.17.1 | ATP-dependent RNA helicase cgh-1; Probable RNA helicase required for oocyte and sperm function. Also required to prevent the physiological germline apoptosis mechanism killing essentially all developing oocytes. Belongs to the DEAD box helicase family. DDX6/DHH1 subfamily. | Cytokinesis, Apoptosis, RNA-associated. | 0.999 |
| cgh-1 | dcap-2 | C07H6.5.1 | F52G2.1b.1 | ATP-dependent RNA helicase cgh-1; Probable RNA helicase required for oocyte and sperm function. Also required to prevent the physiological germline apoptosis mechanism killing essentially all developing oocytes. Belongs to the DEAD box helicase family. DDX6/DHH1 subfamily. | mRNA-decapping enzyme 2; RNA-decapping enzyme although it does not bind cap. May contribute to gene regulation in multiple RNA pathways including monomethylguanosine- and trimethylguanosine-capped RNAs. Belongs to the Nudix hydrolase family. DCP2 subfamily. | 0.998 |
| cgh-1 | edc-3 | C07H6.5.1 | R05D11.8.1 | ATP-dependent RNA helicase cgh-1; Probable RNA helicase required for oocyte and sperm function. Also required to prevent the physiological germline apoptosis mechanism killing essentially all developing oocytes. Belongs to the DEAD box helicase family. DDX6/DHH1 subfamily. | DFDF domain-containing protein. | 0.974 |
| cgh-1 | ifet-1 | C07H6.5.1 | F56F3.1.1 | ATP-dependent RNA helicase cgh-1; Probable RNA helicase required for oocyte and sperm function. Also required to prevent the physiological germline apoptosis mechanism killing essentially all developing oocytes. Belongs to the DEAD box helicase family. DDX6/DHH1 subfamily. | Translational repressor ifet-1; Involved in translational repression of multiple mRNAs in the distal gonad. Recruited to the 3' untranslated region (UTR) of zif-1 by oma-1 and is required for translational repression of zif-1. May also be involved in translational repression of mei-1 through recruitment to the mei-1 3' UTR by oma-1. Required for oogenesis but not spermatogenesis, for P granule formation and for the localization of car-1 and cgh-1 to P granules. Required for normal spindle orientation in early embryos. | 0.999 |
| dcap-2 | Y44E3A.6 | F52G2.1b.1 | Y44E3A.6b.1 | mRNA-decapping enzyme 2; RNA-decapping enzyme although it does not bind cap. May contribute to gene regulation in multiple RNA pathways including monomethylguanosine- and trimethylguanosine-capped RNAs. Belongs to the Nudix hydrolase family. DCP2 subfamily. | FHA domain-containing protein. | 0.989 |
| dcap-2 | car-1 | F52G2.1b.1 | Y18D10A.17.1 | mRNA-decapping enzyme 2; RNA-decapping enzyme although it does not bind cap. May contribute to gene regulation in multiple RNA pathways including monomethylguanosine- and trimethylguanosine-capped RNAs. Belongs to the Nudix hydrolase family. DCP2 subfamily. | Cytokinesis, Apoptosis, RNA-associated. | 0.982 |
| dcap-2 | cgh-1 | F52G2.1b.1 | C07H6.5.1 | mRNA-decapping enzyme 2; RNA-decapping enzyme although it does not bind cap. May contribute to gene regulation in multiple RNA pathways including monomethylguanosine- and trimethylguanosine-capped RNAs. Belongs to the Nudix hydrolase family. DCP2 subfamily. | ATP-dependent RNA helicase cgh-1; Probable RNA helicase required for oocyte and sperm function. Also required to prevent the physiological germline apoptosis mechanism killing essentially all developing oocytes. Belongs to the DEAD box helicase family. DDX6/DHH1 subfamily. | 0.998 |
| dcap-2 | edc-3 | F52G2.1b.1 | R05D11.8.1 | mRNA-decapping enzyme 2; RNA-decapping enzyme although it does not bind cap. May contribute to gene regulation in multiple RNA pathways including monomethylguanosine- and trimethylguanosine-capped RNAs. Belongs to the Nudix hydrolase family. DCP2 subfamily. | DFDF domain-containing protein. | 0.819 |
| edc-3 | Y44E3A.6 | R05D11.8.1 | Y44E3A.6b.1 | DFDF domain-containing protein. | FHA domain-containing protein. | 0.801 |