Disease: Congenital Abnormality
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
TMEM87B Q96K49 transmembrane protein 87B 3.7E-13 0.861 0.115
IP6K1 Q92551 inositol hexakisphosphate kinase 1 Kinase 0.93 0.792 0.269
GJC1 P36383 gap junction protein gamma 1 Cell-cell junction 0.99 0.722 0.385
TBR1 Q16650 T-box brain transcription factor 1 Transcription factor 1.00 0.666 0.385
EML1 O00423 EMAP like 1 1.00 0.705 0.462
HOXD3 P31249 homeobox D3 0.44 0.670 0.462
TCF7L1 Q9HCS4 transcription factor 7 like 1 0.36 0.666 0.462
ARHGAP29 Q52LW3 Rho GTPase activating protein 29 1.00 0.700 0.500
MED13L Q71F56 mediator complex subunit 13L 1.00 0.617 0.538
PDE3A Q14432 phosphodiesterase 3A 1.9E-04 0.670 0.577
ITSN1 Q15811 intersectin 1 Enzyme modulator 1.00 0.656 0.577
BMPR1B O00238 bone morphogenetic protein receptor type 1B Kinase 1.00 0.573 0.615
MEIS1 O00470 Meis homeobox 1 Enzyme 1.00 0.579 0.615
MYH6 P13533 myosin heavy chain 6 1.6E-32 0.581 0.615
WNT2B Q93097 Wnt family member 2B Signaling 3.8E-02 0.644 0.615
CFDP1 Q9UEE9 craniofacial development protein 1 3.7E-03 0.619 0.615
WWP2 O00308 WW domain containing E3 ubiquitin protein ligase 2 Enzyme 0.16 0.650 0.615
GATA2 P23769 GATA binding protein 2 0.98 0.496 0.654
NRIP1 P48552 nuclear receptor interacting protein 1 0.99 0.592 0.654
SLC9A3R2 Q15599 SLC9A3 regulator 2 3.8E-02 0.588 0.654
ALG9 Q9H6U8 ALG9 alpha-1,2-mannosyltransferase Enzyme 6.4E-04 0.644 0.654
GLIS3 Q8NEA6 GLIS family zinc finger 3 5.6E-08 0.590 0.654
HOXA11 P31270 homeobox A11 0.94 0.568 0.692
LRP4 O75096 LDL receptor related protein 4 1.4E-06 0.568 0.692
NRXN1 P58400 Q9ULB1 neurexin 1 1.00 0.581 0.692