Disease: Congenital Abnormality
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
ABCD1 P33897 ATP binding cassette subfamily D member 1 Transporter 1.00 0.563 0.731
ACTB P60709 actin beta Cellular structure 0.99 0.325 0.923
ADORA2A P29274 adenosine A2a receptor G-protein coupled receptor 0.60 0.526 0.769
AHI1 Q8N157 Abelson helper integration site 1 1.1E-25 0.513 0.846
AHR P35869 aryl hydrocarbon receptor Transcription factor 1.00 0.410 0.923
ALMS1 Q8TCU4 ALMS1 centrosome and basal body associated protein 4.5E-60 0.559 0.808
ARL13B Q3SXY8 ADP ribosylation factor like GTPase 13B 2.7E-09 0.631 0.538
ARNT2 Q9HBZ2 aryl hydrocarbon receptor nuclear translocator 2 Transcription factor 0.99 0.599 0.731
ASRGL1 Q7L266 asparaginase and isoaspartyl peptidase 1 Enzyme 2.8E-05 0.494 0.808
ATF6 P18850 activating transcription factor 6 3.2E-07 0.516 0.846
ATF6B Q99941 activating transcription factor 6 beta 3.1E-07 0.839 0.192
ATRX P46100 ATRX chromatin remodeler 1.00 0.452 0.808
ATXN7 O15265 ataxin 7 0.96 0.581 0.654
AVP P01185 arginine vasopressin Signaling 7.4E-02 0.437 0.846
BBS2 Q9BXC9 Bardet-Biedl syndrome 2 1.0E-17 0.565 0.654
BDNF P23560 brain derived neurotrophic factor Signaling 0.66 0.345 0.923
BMP4 P12644 bone morphogenetic protein 4 Signaling 0.96 0.422 0.808
BRCA1 P38398 BRCA1 DNA repair associated Enzyme 9.2E-29 0.367 0.923
CACNA1C Q13936 calcium voltage-gated channel subunit alpha1 C Ion channel 1.00 0.510 0.846
CDH23 Q9H251 cadherin related 23 3.2E-06 0.539 0.769
CEP290 O15078 centrosomal protein 290 1.1E-60 0.517 0.769
CFH P08603 complement factor H 0.86 0.441 0.885
CKAP4 Q07065 cytoskeleton associated protein 4 0.51 0.436 0.731
CRB2 Q5IJ48 crumbs cell polarity complex component 2 1.5E-14 0.678 0.269
CSF2 P04141 colony stimulating factor 2 Signaling 0.83 0.330 0.962