Disease: Congenital Abnormality
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
AHI1 Q8N157 Abelson helper integration site 1 1.1E-25 0.513 0.846
AKT3 Q9Y243 AKT serine/threonine kinase 3 Kinase 1.00 0.512 0.808
ALMS1 Q8TCU4 ALMS1 centrosome and basal body associated protein 4.5E-60 0.559 0.808
ALX3 O95076 ALX homeobox 3 1.9E-02 0.578 0.692
BBS2 Q9BXC9 Bardet-Biedl syndrome 2 1.0E-17 0.565 0.654
BMP4 P12644 bone morphogenetic protein 4 Signaling 0.96 0.422 0.808
BRD2 P25440 bromodomain containing 2 Epigenetic regulator 1.00 0.450 0.808
C2CD3 Q4AC94 C2 domain containing 3 centriole elongation regulator 4.4E-19 0.636 0.538
CENPF P49454 centromere protein F 1.9E-36 0.601 0.654
CEP290 O15078 centrosomal protein 290 1.1E-60 0.517 0.769
CILK1 Q9UPZ9 ciliogenesis associated kinase 1 Kinase 1.3E-05 0.545 0.808
CPLANE1 Q9H799 ciliogenesis and planar polarity effector 1 5.9E-36 0.575 0.692
CREBBP Q92793 CREB binding protein 1.00 0.428 0.808
DEL11P13 Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome 0.716 0.538
DHCR7 Q9UBM7 7-dehydrocholesterol reductase Enzyme 3.9E-13 0.500 0.846
EBP Q15125 EBP cholestenol delta-isomerase Enzyme 0.94 0.494 0.846
ELN P15502 elastin 2.1E-14 0.415 0.885
EP300 Q09472 E1A binding protein p300 1.00 0.459 0.846
EVC2 Q86UK5 EvC ciliary complex subunit 2 1.0E-34 0.585 0.692
FBXW11 Q9UKB1 F-box and WD repeat domain containing 11 0.98 0.626 0.462
FGF10 O15520 fibroblast growth factor 10 Signaling 0.94 0.530 0.692
FGFR1 P11362 fibroblast growth factor receptor 1 Kinase 1.00 0.362 0.885
FGFR2 P21802 fibroblast growth factor receptor 2 Kinase 1.00 0.380 0.808
FGFR3 P22607 fibroblast growth factor receptor 3 Kinase 1.6E-05 0.391 0.846
FOXA2 Q9Y261 forkhead box A2 Transcription factor 0.74 0.528 0.769