Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 115482693
Gene Symbol: H3P8
H3P8
H3 histone pseudogene 8 0.544 0.808
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 1998 1998
Entrez Id: 115482706
Gene Symbol: H3P47
H3P47
H3 histone pseudogene 47 0.603 0.538
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2011 2011
Entrez Id: 115482713
Gene Symbol: H3P10
H3P10
H3 histone pseudogene 10 0.350 0.846
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 117195
Gene Symbol: MRGPRX3
MRGPRX3
MAS related GPR family member X3 0.529 0.923
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2005 2005
Entrez Id: 117196
Gene Symbol: MRGPRX4
MRGPRX4
MAS related GPR family member X4 0.531 0.923
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2005 2005
Entrez Id: 126
Gene Symbol: ADH1C
ADH1C
alcohol dehydrogenase 1C (class I), gamma polypeptide 0.547 0.731
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2001 2001
Entrez Id: 139189
Gene Symbol: DGKK
DGKK
diacylglycerol kinase kappa 0.780 0.385
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 170
Gene Symbol: AFA
AFA
ankyloblepharon filiforme adnatum 0.792 0.462
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2010 2010
Entrez Id: 259249
Gene Symbol: MRGPRX1
MRGPRX1
MAS related GPR family member X1 0.531 0.923
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2005 2005
Entrez Id: 266719
Gene Symbol: RRDX
RRDX
Radial ray deficiency 0.805 0.154
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2013 2013
Entrez Id: 2728
Gene Symbol: GLC3B
GLC3B
glaucoma 3, primary infantile, B 0.769 0.154
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None < 0.001 1 0 2011 2011
Entrez Id: 3197
Gene Symbol: HOXA@
HOXA@
homeobox A cluster 0.599 0.654
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2011 2011
Entrez Id: 3210
Gene Symbol: HOXB@
HOXB@
homeobox B cluster 0.631 0.538
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2007 2007
Entrez Id: 3220
Gene Symbol: HOXC@
HOXC@
homeobox C cluster 0.695 0.462
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2016 2016
Entrez Id: 339476
Gene Symbol: ERVMER61-1
ERVMER61-1
endogenous retrovirus group MER61 member 1 0.890 0.115
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None < 0.001 1 0 2013 2013
Entrez Id: 399565
Gene Symbol: GLC3C
GLC3C
glaucoma 3, primary congenital, C 1.000 0.115
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None < 0.001 1 0 2011 2011
Entrez Id: 406985
Gene Symbol: MIR200C
MIR200C
microRNA 200c 0.486 0.846
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2013 2013
Entrez Id: 407975
Gene Symbol: MIR17HG
MIR17HG
miR-17-92a-1 cluster host gene 0.483 0.808
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2011 2011
Entrez Id: 441931
Gene Symbol: VN1R17P
VN1R17P
vomeronasal 1 receptor 17 pseudogene 0.529 0.923
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2005 2005
Entrez Id: 442206
Gene Symbol: GPR166P
GPR166P
G protein-coupled receptor 166 pseudogene 0.531 0.923
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2005 2005
Entrez Id: 4567
Gene Symbol: TRNL1
TRNL1
tRNA 0.534 0.731
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2013 2013
Entrez Id: 470
Gene Symbol: ATHS
ATHS
atherosclerosis susceptibility (lipoprotein associated) 0.551 0.769
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2019 2019
Entrez Id: 4964
Gene Symbol: OFC2
OFC2
orofacial cleft 2 0.931 0.115
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 1998 1998
Entrez Id: 51072
Gene Symbol: MEMO1
MEMO1
mediator of cell motility 1 0.705 0.346
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2016 2016
Entrez Id: 5175
Gene Symbol: PECAM1
PECAM1
platelet and endothelial cell adhesion molecule 1 0.426 0.846
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
group 0.010 None 1.000 1 0 2015 2015