Disease: Clumsiness - motor delay
Source: INFERRED ×
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
FRRS1L Q9P0K9 ferric chelate reductase 1 like 1.5E-03 0.666 0.231
LINS1 Q8NG48 lines homolog 1 2.4E-07 0.691 0.231
METTL23 Q86XA0 methyltransferase like 23 1.3E-07 0.682 0.231
SLC45A1 Q9Y2W3 solute carrier family 45 member 1 Transporter 2.5E-05 0.674 0.269
PRSS12 P56730 serine protease 12 Enzyme 8.4E-29 0.682 0.308
C12orf4 Q9NQ89 chromosome 12 open reading frame 4 1.1E-05 0.691 0.308
ZC3H14 Q6PJT7 zinc finger CCCH-type containing 14 0.88 0.691 0.308
EDC3 Q96F86 enhancer of mRNA decapping 3 2.6E-02 0.682 0.308
ALG14 Q96F25 ALG14 UDP-N-acetylglucosaminyltransferase subunit 9.4E-04 0.722 0.308
PIGC Q92535 phosphatidylinositol glycan anchor biosynthesis class C Enzyme 5.5E-03 0.691 0.346
WASHC4 Q2M389 WASH complex subunit 4 2.8E-06 0.686 0.346
FDX2 Q6P4F2 ferredoxin 2 1.7E-03 0.780 0.346
CLCNKA P51800 chloride voltage-gated channel Ka Ion channel 4.2E-17 0.711 0.385
DYNC1I2 Q13409 dynein cytoplasmic 1 intermediate chain 2 Cellular structure 1.1E-08 0.760 0.385
SPEG Q15772 striated muscle enriched protein kinase Kinase 0.92 0.686 0.385
KCNK4 Q9NYG8 potassium two pore domain channel subfamily K member 4 Ion channel 5.7E-03 0.743 0.385
LMAN2L Q9H0V9 lectin, mannose binding 2 like Transporter 2.0E-11 0.641 0.385
KBTBD13 C9JR72 kelch repeat and BTB domain containing 13 2.3E-10 0.729 0.385
IPW imprinted in Prader-Willi syndrome 0.682 0.423
TECR Q9NZ01 trans-2,3-enoyl-CoA reductase Enzyme 0.11 0.674 0.423
MKRN3-AS1 MKRN3 antisense RNA 1 0.682 0.423
LMOD3 Q0VAK6 leiomodin 3 Cellular structure 1.6E-07 0.700 0.423
FBXO31 Q5XUX0 F-box protein 31 0.44 0.653 0.423
PGAP1 Q75T13 post-GPI attachment to proteins inositol deacylase 1 Transporter 3.2E-08 0.650 0.423
ALG2 Q9H553 ALG2 alpha-1,3/1,6-mannosyltransferase 8.0E-05 0.670 0.423