Disease: Multiple congenital anomalies
Source: INFERRED ×
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
ZSWIM6 Q9HCJ5 zinc finger SWIM-type containing 6 1.00 0.626 0.577
ZMYND11 Q15326 zinc finger MYND-type containing 11 1.00 0.647 0.500
ZEB2 O60315 zinc finger E-box binding homeobox 2 Transcription factor 1.00 0.471 0.808
ZC4H2 Q9NQZ6 zinc finger C4H2-type containing 0.91 0.561 0.731
ZBTB18 Q99592 zinc finger and BTB domain containing 18 Transcription factor 1.00 0.666 0.500
XYLT2 Q9H1B5 xylosyltransferase 2 0.93 0.566 0.808
WDR45 Q9Y484 WD repeat domain 45 0.99 0.647 0.423
WDR26 Q9H7D7 WD repeat domain 26 1.00 0.606 0.769
WAC Q9BTA9 WW domain containing adaptor with coiled-coil 1.00 0.686 0.615
VAX2 Q9UIW0 ventral anterior homeobox 2 Transcription factor 0.16 0.769 0.308
UBE3B Q7Z3V4 ubiquitin protein ligase E3B 4.2E-08 0.590 0.692
TUBB P07437 tubulin beta class I Cellular structure 0.98 0.603 0.692
TUBA1A Q71U36 tubulin alpha 1a Cellular structure 0.97 0.597 0.769
TRPV4 Q9HBA0 transient receptor potential cation channel subfamily V member 4 Ion channel 2.2E-16 0.457 0.808
TRPS1 Q9UHF7 transcriptional repressor GATA binding 1 1.00 0.537 0.769
TRMU O75648 tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase 1.5E-16 0.716 0.385
TRIO O75962 trio Rho guanine nucleotide exchange factor Kinase 1.00 0.556 0.731
TMEM67 Q5HYA8 transmembrane protein 67 2.1E-24 0.512 0.769
TMEM216 Q9P0N5 transmembrane protein 216 1.9E-03 0.544 0.615
TMEM151B Q8IW70 transmembrane protein 151B 0.14 0.792 0.346
TMCO1 Q9UM00 transmembrane and coiled-coil domains 1 9.4E-10 0.588 0.654
THRA P10827 thyroid hormone receptor alpha Nuclear receptor 0.33 0.566 0.769
THOC6 Q86W42 THO complex 6 4.8E-04 0.705 0.577
TFAP2A P05549 transcription factor AP-2 alpha Transcription factor 0.99 0.488 0.769
TBCE Q15813 tubulin folding cofactor E Chaperone 1.7E-08 0.575 0.692