| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| C1orf109 | CINP | ENSPPYP00000001763 | ENSPPYP00000007000 | Chromosome 1 open reading frame 109. | Cyclin dependent kinase 2 interacting protein. | 0.925 |
| C1orf109 | SPATA5 | ENSPPYP00000001763 | ENSPPYP00000016811 | Chromosome 1 open reading frame 109. | SPATA5 isoform 1. | 0.848 |
| C1orf109 | SPATA5L1 | ENSPPYP00000001763 | ENSPPYP00000007302 | Chromosome 1 open reading frame 109. | SPATA5L1 isoform 1. | 0.936 |
| CINP | C1orf109 | ENSPPYP00000007000 | ENSPPYP00000001763 | Cyclin dependent kinase 2 interacting protein. | Chromosome 1 open reading frame 109. | 0.925 |
| CINP | NSA2 | ENSPPYP00000007000 | ENSPPYP00000023551 | Cyclin dependent kinase 2 interacting protein. | NSA2 isoform 1. | 0.776 |
| CINP | SPATA5 | ENSPPYP00000007000 | ENSPPYP00000016811 | Cyclin dependent kinase 2 interacting protein. | SPATA5 isoform 1. | 0.936 |
| CINP | SPATA5L1 | ENSPPYP00000007000 | ENSPPYP00000007302 | Cyclin dependent kinase 2 interacting protein. | SPATA5L1 isoform 1. | 0.936 |
| DERL1 | PSMD2 | ENSPPYP00000021151 | ENSPPYP00000016052 | Derlin-1; Functional component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins. May act by forming a channel that allows the retrotranslocation of misfolded proteins into the cytosol where they are ubiquitinated and degraded by the proteasome. May mediate the interaction between VCP and the misfolded protein. Also involved in endoplasmic reticulum stress-induced pre- emptive quality control, a mechanism that selectively attenuates the translocation of newly synthesized proteins into the endoplasmic reticulum and reroutes them to the cytosol for pro [...] | 26S proteasome non-ATPase regulatory subunit 2; Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. | 0.405 |
| DERL1 | SPATA5 | ENSPPYP00000021151 | ENSPPYP00000016811 | Derlin-1; Functional component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins. May act by forming a channel that allows the retrotranslocation of misfolded proteins into the cytosol where they are ubiquitinated and degraded by the proteasome. May mediate the interaction between VCP and the misfolded protein. Also involved in endoplasmic reticulum stress-induced pre- emptive quality control, a mechanism that selectively attenuates the translocation of newly synthesized proteins into the endoplasmic reticulum and reroutes them to the cytosol for pro [...] | SPATA5 isoform 1. | 0.829 |
| DERL1 | SPATA5L1 | ENSPPYP00000021151 | ENSPPYP00000007302 | Derlin-1; Functional component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins. May act by forming a channel that allows the retrotranslocation of misfolded proteins into the cytosol where they are ubiquitinated and degraded by the proteasome. May mediate the interaction between VCP and the misfolded protein. Also involved in endoplasmic reticulum stress-induced pre- emptive quality control, a mechanism that selectively attenuates the translocation of newly synthesized proteins into the endoplasmic reticulum and reroutes them to the cytosol for pro [...] | SPATA5L1 isoform 1. | 0.829 |
| DERL1 | UBXN1 | ENSPPYP00000021151 | ENSPPYP00000003643 | Derlin-1; Functional component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins. May act by forming a channel that allows the retrotranslocation of misfolded proteins into the cytosol where they are ubiquitinated and degraded by the proteasome. May mediate the interaction between VCP and the misfolded protein. Also involved in endoplasmic reticulum stress-induced pre- emptive quality control, a mechanism that selectively attenuates the translocation of newly synthesized proteins into the endoplasmic reticulum and reroutes them to the cytosol for pro [...] | UBXN1 isoform 1. | 0.958 |
| DERL1 | UFD1 | ENSPPYP00000021151 | ENSPPYP00000012917 | Derlin-1; Functional component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins. May act by forming a channel that allows the retrotranslocation of misfolded proteins into the cytosol where they are ubiquitinated and degraded by the proteasome. May mediate the interaction between VCP and the misfolded protein. Also involved in endoplasmic reticulum stress-induced pre- emptive quality control, a mechanism that selectively attenuates the translocation of newly synthesized proteins into the endoplasmic reticulum and reroutes them to the cytosol for pro [...] | Ubiquitin recognition factor in ER associated degradation 1. | 0.864 |
| NSA2 | CINP | ENSPPYP00000023551 | ENSPPYP00000007000 | NSA2 isoform 1. | Cyclin dependent kinase 2 interacting protein. | 0.776 |
| NSA2 | SPATA5 | ENSPPYP00000023551 | ENSPPYP00000016811 | NSA2 isoform 1. | SPATA5 isoform 1. | 0.808 |
| NSA2 | SPATA5L1 | ENSPPYP00000023551 | ENSPPYP00000007302 | NSA2 isoform 1. | SPATA5L1 isoform 1. | 0.785 |
| PSMD2 | DERL1 | ENSPPYP00000016052 | ENSPPYP00000021151 | 26S proteasome non-ATPase regulatory subunit 2; Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. | Derlin-1; Functional component of endoplasmic reticulum-associated degradation (ERAD) for misfolded lumenal proteins. May act by forming a channel that allows the retrotranslocation of misfolded proteins into the cytosol where they are ubiquitinated and degraded by the proteasome. May mediate the interaction between VCP and the misfolded protein. Also involved in endoplasmic reticulum stress-induced pre- emptive quality control, a mechanism that selectively attenuates the translocation of newly synthesized proteins into the endoplasmic reticulum and reroutes them to the cytosol for pro [...] | 0.405 |
| PSMD2 | SPATA5 | ENSPPYP00000016052 | ENSPPYP00000016811 | 26S proteasome non-ATPase regulatory subunit 2; Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. | SPATA5 isoform 1. | 0.835 |
| PSMD2 | SPATA5L1 | ENSPPYP00000016052 | ENSPPYP00000007302 | 26S proteasome non-ATPase regulatory subunit 2; Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. | SPATA5L1 isoform 1. | 0.835 |
| PSMD2 | UBXN7 | ENSPPYP00000016052 | ENSPPYP00000016149 | 26S proteasome non-ATPase regulatory subunit 2; Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. | UBX domain-containing protein 7; Ubiquitin-binding adapter that links a subset of NEDD8- associated cullin ring ligases (CRLs) to the segregase VCP/p97, to regulate turnover of their ubiquitination substrates (By similarity). | 0.825 |
| PSMD2 | UFD1 | ENSPPYP00000016052 | ENSPPYP00000012917 | 26S proteasome non-ATPase regulatory subunit 2; Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. | Ubiquitin recognition factor in ER associated degradation 1. | 0.602 |
