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: 64218
Gene Symbol: SEMA4A
SEMA4A
semaphorin 4A 0.569 0.692 1.8E-05
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 56262
Gene Symbol: LRRC8A
LRRC8A
leucine rich repeat containing 8 VRAC subunit A 0.644 0.692 0.94
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 55670
Gene Symbol: PEX26
PEX26
peroxisomal biogenesis factor 26 0.584 0.615 0.93
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 55651
Gene Symbol: NHP2
NHP2
NHP2 ribonucleoprotein 0.623 0.654 5.0E-02
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 55630
Gene Symbol: SLC39A4
SLC39A4
solute carrier family 39 member 4 0.628 0.692 3.1E-04
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 55505
Gene Symbol: NOP10
NOP10
NOP10 ribonucleoprotein 0.631 0.654 0.77
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 55315
Gene Symbol: SLC29A3
SLC29A3
solute carrier family 29 member 3 0.578 0.769 1.3E-07
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 55135
Gene Symbol: WRAP53
WRAP53
WD repeat containing antisense to TP53 0.603 0.692 5.4E-05
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 54888
Gene Symbol: NSUN2
NSUN2
NOP2/Sun RNA methyltransferase 2 0.559 0.846 2.6E-04
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 567
Gene Symbol: B2M
B2M
beta-2-microglobulin 0.447 0.846 0.56
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 57570
Gene Symbol: TRMT5
TRMT5
tRNA methyltransferase 5 0.769 0.231 5.0E-02
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5824
Gene Symbol: PEX19
PEX19
peroxisomal biogenesis factor 19 0.585 0.731 3.2E-04
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 6288
Gene Symbol: SAA1
SAA1
serum amyloid A1 0.513 0.808 1.5E-02
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 6224
Gene Symbol: RPS20
RPS20
ribosomal protein S20 0.610 0.692 2.1E-02
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
RNA component of mitochondrial RNA processing endoribonuclease 0.519 0.731
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5994
Gene Symbol: RFXAP
RFXAP
regulatory factor X associated protein 0.663 0.577 2.3E-02
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5993
Gene Symbol: RFX5
RFX5
regulatory factor X5 0.650 0.577 2.0E-11
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5982
Gene Symbol: RFC2
RFC2
replication factor C subunit 2 0.520 0.769 2.2E-06
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5830
Gene Symbol: PEX5
PEX5
peroxisomal biogenesis factor 5 0.561 0.731 5.6E-05
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5828
Gene Symbol: PEX2
PEX2
peroxisomal biogenesis factor 2 0.582 0.654 2.6E-04
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5428
Gene Symbol: POLG
POLG
DNA polymerase gamma, catalytic subunit 0.457 0.846 2.1E-09
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5395
Gene Symbol: PMS2
PMS2
PMS1 homolog 2, mismatch repair system component 0.484 0.808 4.5E-27
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 538
Gene Symbol: ATP7A
ATP7A
ATPase copper transporting alpha 0.494 0.769 1.00
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 51750
Gene Symbol: RTEL1
RTEL1
regulator of telomere elongation helicase 1 0.459 0.808 8.9E-10
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 5167
Gene Symbol: ENPP1
ENPP1
ectonucleotide pyrophosphatase/phosphodiesterase 1 0.498 0.808 5.0E-08
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype 0.100 None 0 0