node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
ABCG4 | LRRC73 | ENSP00000481728 | ENSP00000361518 | ATP-binding cassette sub-family G member 4; May be involved in macrophage lipid homeostasis; ATP binding cassette subfamily G | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | 0.469 |
ADPRHL2 | C1orf85 | ENSP00000362273 | ENSP00000354553 | Poly(ADP-ribose) glycohydrolase ARH3; Poly(ADP-ribose) synthesized after DNA damage is only present transiently and is rapidly degraded by poly(ADP-ribose) glycohydrolase. Poly(ADP-ribose) metabolism may be required for maintenance of the normal function of neuronal cells. Generates ADP-ribose from poly-(ADP-ribose), but does not hydrolyze ADP- ribose-arginine, -cysteine, -diphthamide, or -asparagine bonds. Due to catalytic inactivity of PARG mitochondrial isoforms, ARH3 is the only PAR hydrolyzing enzyme in mitochondria | Glycosylated lysosomal membrane protein; Chromosome 1 open reading frame 85; Belongs to the GLMP family | 0.452 |
ADPRHL2 | CEP85 | ENSP00000362273 | ENSP00000252992 | Poly(ADP-ribose) glycohydrolase ARH3; Poly(ADP-ribose) synthesized after DNA damage is only present transiently and is rapidly degraded by poly(ADP-ribose) glycohydrolase. Poly(ADP-ribose) metabolism may be required for maintenance of the normal function of neuronal cells. Generates ADP-ribose from poly-(ADP-ribose), but does not hydrolyze ADP- ribose-arginine, -cysteine, -diphthamide, or -asparagine bonds. Due to catalytic inactivity of PARG mitochondrial isoforms, ARH3 is the only PAR hydrolyzing enzyme in mitochondria | Centrosomal protein of 85 kDa; Acts as a negative regulator of NEK2 to maintain the centrosome integrity in interphase. Suppresses centrosome disjunction by inhibiting NEK2 kinase activity; Belongs to the CEP85 family | 0.560 |
ADPRHL2 | LRRC73 | ENSP00000362273 | ENSP00000361518 | Poly(ADP-ribose) glycohydrolase ARH3; Poly(ADP-ribose) synthesized after DNA damage is only present transiently and is rapidly degraded by poly(ADP-ribose) glycohydrolase. Poly(ADP-ribose) metabolism may be required for maintenance of the normal function of neuronal cells. Generates ADP-ribose from poly-(ADP-ribose), but does not hydrolyze ADP- ribose-arginine, -cysteine, -diphthamide, or -asparagine bonds. Due to catalytic inactivity of PARG mitochondrial isoforms, ARH3 is the only PAR hydrolyzing enzyme in mitochondria | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | 0.451 |
ADPRHL2 | TMEM208 | ENSP00000362273 | ENSP00000305892 | Poly(ADP-ribose) glycohydrolase ARH3; Poly(ADP-ribose) synthesized after DNA damage is only present transiently and is rapidly degraded by poly(ADP-ribose) glycohydrolase. Poly(ADP-ribose) metabolism may be required for maintenance of the normal function of neuronal cells. Generates ADP-ribose from poly-(ADP-ribose), but does not hydrolyze ADP- ribose-arginine, -cysteine, -diphthamide, or -asparagine bonds. Due to catalytic inactivity of PARG mitochondrial isoforms, ARH3 is the only PAR hydrolyzing enzyme in mitochondria | Transmembrane protein 208; May function as a negative regulator of endoplasmic reticulum-stress induced autophagy | 0.524 |
C17orf51 | LRRC73 | ENSP00000384286 | ENSP00000361518 | Uncharacterized protein C17orf51; Chromosome 17 open reading frame 51 | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | 0.477 |
C17orf51 | OR4C46 | ENSP00000384286 | ENSP00000329056 | Uncharacterized protein C17orf51; Chromosome 17 open reading frame 51 | Olfactory receptor 4C46; Odorant receptor; Olfactory receptors, family 4 | 0.570 |
C1orf85 | ADPRHL2 | ENSP00000354553 | ENSP00000362273 | Glycosylated lysosomal membrane protein; Chromosome 1 open reading frame 85; Belongs to the GLMP family | Poly(ADP-ribose) glycohydrolase ARH3; Poly(ADP-ribose) synthesized after DNA damage is only present transiently and is rapidly degraded by poly(ADP-ribose) glycohydrolase. Poly(ADP-ribose) metabolism may be required for maintenance of the normal function of neuronal cells. Generates ADP-ribose from poly-(ADP-ribose), but does not hydrolyze ADP- ribose-arginine, -cysteine, -diphthamide, or -asparagine bonds. Due to catalytic inactivity of PARG mitochondrial isoforms, ARH3 is the only PAR hydrolyzing enzyme in mitochondria | 0.452 |
C1orf85 | CEP85 | ENSP00000354553 | ENSP00000252992 | Glycosylated lysosomal membrane protein; Chromosome 1 open reading frame 85; Belongs to the GLMP family | Centrosomal protein of 85 kDa; Acts as a negative regulator of NEK2 to maintain the centrosome integrity in interphase. Suppresses centrosome disjunction by inhibiting NEK2 kinase activity; Belongs to the CEP85 family | 0.521 |
C1orf85 | LRRC73 | ENSP00000354553 | ENSP00000361518 | Glycosylated lysosomal membrane protein; Chromosome 1 open reading frame 85; Belongs to the GLMP family | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | 0.450 |
C1orf85 | TMEM208 | ENSP00000354553 | ENSP00000305892 | Glycosylated lysosomal membrane protein; Chromosome 1 open reading frame 85; Belongs to the GLMP family | Transmembrane protein 208; May function as a negative regulator of endoplasmic reticulum-stress induced autophagy | 0.463 |
CEP85 | ADPRHL2 | ENSP00000252992 | ENSP00000362273 | Centrosomal protein of 85 kDa; Acts as a negative regulator of NEK2 to maintain the centrosome integrity in interphase. Suppresses centrosome disjunction by inhibiting NEK2 kinase activity; Belongs to the CEP85 family | Poly(ADP-ribose) glycohydrolase ARH3; Poly(ADP-ribose) synthesized after DNA damage is only present transiently and is rapidly degraded by poly(ADP-ribose) glycohydrolase. Poly(ADP-ribose) metabolism may be required for maintenance of the normal function of neuronal cells. Generates ADP-ribose from poly-(ADP-ribose), but does not hydrolyze ADP- ribose-arginine, -cysteine, -diphthamide, or -asparagine bonds. Due to catalytic inactivity of PARG mitochondrial isoforms, ARH3 is the only PAR hydrolyzing enzyme in mitochondria | 0.560 |
CEP85 | C1orf85 | ENSP00000252992 | ENSP00000354553 | Centrosomal protein of 85 kDa; Acts as a negative regulator of NEK2 to maintain the centrosome integrity in interphase. Suppresses centrosome disjunction by inhibiting NEK2 kinase activity; Belongs to the CEP85 family | Glycosylated lysosomal membrane protein; Chromosome 1 open reading frame 85; Belongs to the GLMP family | 0.521 |
CEP85 | LRRC73 | ENSP00000252992 | ENSP00000361518 | Centrosomal protein of 85 kDa; Acts as a negative regulator of NEK2 to maintain the centrosome integrity in interphase. Suppresses centrosome disjunction by inhibiting NEK2 kinase activity; Belongs to the CEP85 family | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | 0.519 |
CEP85 | TMEM208 | ENSP00000252992 | ENSP00000305892 | Centrosomal protein of 85 kDa; Acts as a negative regulator of NEK2 to maintain the centrosome integrity in interphase. Suppresses centrosome disjunction by inhibiting NEK2 kinase activity; Belongs to the CEP85 family | Transmembrane protein 208; May function as a negative regulator of endoplasmic reticulum-stress induced autophagy | 0.576 |
ELFN1 | LRRC73 | ENSP00000456548 | ENSP00000361518 | Protein ELFN1; Postsynaptic protein that regulates circuit dynamics in the central nervous system by modulating the temporal dynamics of interneuron recruitment. Specifically present in excitatory synapses onto oriens-lacunosum molecular (OLM) interneurons and acts as a regulator of presynaptic release probability to direct the formation of highly facilitating pyramidal-OLM synapses (By similarity). Inhibits phosphatase activity of protein phosphatase 1 (PP1) complexes; Fibronectin type III domain containing | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | 0.577 |
JPH3 | LRRC73 | ENSP00000284262 | ENSP00000361518 | Junctophilin-3; Junctophilins contribute to the formation of junctional membrane complexes (JMCs) which link the plasma membrane with the endoplasmic or sarcoplasmic reticulum in excitable cells. Provides a structural foundation for functional cross-talk between the cell surface and intracellular calcium release channels. JPH3 is brain- specific and appears to have an active role in certain neurons involved in motor coordination and memory | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | 0.512 |
LRRC73 | ABCG4 | ENSP00000361518 | ENSP00000481728 | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | ATP-binding cassette sub-family G member 4; May be involved in macrophage lipid homeostasis; ATP binding cassette subfamily G | 0.469 |
LRRC73 | ADPRHL2 | ENSP00000361518 | ENSP00000362273 | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | Poly(ADP-ribose) glycohydrolase ARH3; Poly(ADP-ribose) synthesized after DNA damage is only present transiently and is rapidly degraded by poly(ADP-ribose) glycohydrolase. Poly(ADP-ribose) metabolism may be required for maintenance of the normal function of neuronal cells. Generates ADP-ribose from poly-(ADP-ribose), but does not hydrolyze ADP- ribose-arginine, -cysteine, -diphthamide, or -asparagine bonds. Due to catalytic inactivity of PARG mitochondrial isoforms, ARH3 is the only PAR hydrolyzing enzyme in mitochondria | 0.451 |
LRRC73 | C17orf51 | ENSP00000361518 | ENSP00000384286 | Leucine-rich repeat-containing protein 73; Leucine rich repeat containing 73 | Uncharacterized protein C17orf51; Chromosome 17 open reading frame 51 | 0.477 |