Disease: Congenital muscular dystrophy (disorder)
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
TGFB1 P01137 transforming growth factor beta 1 Signaling 3.7E-02 0.287 0.962
MIR21 microRNA 21 0.363 0.846
TIMP1 P01033 TIMP metallopeptidase inhibitor 1 Enzyme modulator 0.50 0.380 0.885
LMNA P02545 lamin A/C 1.00 0.384 0.885
DMD P11532 dystrophin 1.00 0.423 0.923
SMN1 Q16637 survival of motor neuron 1, telomeric Epigenetic regulator 1.6E-02 0.454 0.769
TTN Q8WZ42 titin Kinase 2.6E-96 0.470 0.885
BGN P21810 biglycan 0.45 0.484 0.808
RYR1 P21817 ryanodine receptor 1 Ion channel 1.6E-29 0.489 0.808
DAG1 Q14118 dystroglycan 1 Receptor 0.98 0.498 0.808
FKTN O75072 fukutin 8.7E-07 0.511 0.692
SYNE1 Q8NF91 spectrin repeat containing nuclear envelope protein 1 3.2E-52 0.511 0.846
FKRP Q9H9S5 fukutin related protein 9.8E-06 0.513 0.731
POMT1 Q9Y6A1 protein O-mannosyltransferase 1 4.2E-17 0.525 0.615
LARGE1 O95461 LARGE xylosyl- and glucuronyltransferase 1 Enzyme 0.99 0.526 0.654
POMGNT1 Q8WZA1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) 1.9E-20 0.537 0.538
POMT2 Q9UKY4 protein O-mannosyltransferase 2 9.4E-12 0.544 0.615
LAMA2 P24043 laminin subunit alpha 2 Enzyme modulator 2.4E-47 0.553 0.692
COL6A3 P12111 collagen type VI alpha 3 chain Receptor 1.8E-20 0.563 0.769
CAPN3 P20807 calpain 3 Enzyme 3.6E-19 0.564 0.615
CRPPA A4D126 CDP-L-ribitol pyrophosphorylase A 2.5E-04 0.566 0.654
SELENON Q9NZV5 selenoprotein N 9.8E-10 0.575 0.692
GMPPB Q9Y5P6 GDP-mannose pyrophosphorylase B 8.4E-07 0.578 0.538
B3GALNT2 Q8NCR0 beta-1,3-N-acetylgalactosaminyltransferase 2 Enzyme 2.8E-07 0.578 0.577
MSTO1 Q9BUK6 misato mitochondrial distribution and morphology regulator 1 1.6E-09 0.582 0.692