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: 6347
Gene Symbol: CCL2
CCL2
C-C motif chemokine ligand 2 0.321 0.962 0.61
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.020 None 1.000 2 0 2017 2019
Entrez Id: 6647
Gene Symbol: SOD1
SOD1
superoxide dismutase 1 0.379 0.962 0.18
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.020 None 1.000 2 0 2011 2019
Entrez Id: 1437
Gene Symbol: CSF2
CSF2
colony stimulating factor 2 0.330 0.962 0.83
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
prion protein 0.445 0.923 6.3E-04
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 1.000 20 1 1993 2018
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
phosphatase and tensin homolog 0.305 0.923 0.26
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 1.000 14 1 2001 2015
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
microtubule associated protein tau 0.446 0.923 6.0E-03
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.070 None 1.000 7 0 2000 2015
Entrez Id: 5265
Gene Symbol: SERPINA1
SERPINA1
serpin family A member 1 0.410 0.923 6.8E-08
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 1.000 6 1 1983 2015
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
cytochrome P450 family 1 subfamily A member 2 0.494 0.923 2.5E-10
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.010 None 1.000 1 0 2012 2012
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 5594
Gene Symbol: MAPK1
MAPK1
mitogen-activated protein kinase 1 0.330 0.923 1.00
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1
catenin beta 1 0.303 0.885 1.00
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 1.000 22 3 1991 2017
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
lysine methyltransferase 2A 0.410 0.885 1.00
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 1.000 22 3 1989 2017
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
synuclein alpha 0.427 0.885 0.88
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 0.941 17 2 2002 2020
Entrez Id: 6687
Gene Symbol: SPG7
SPG7
SPG7 matrix AAA peptidase subunit, paraplegin 0.436 0.885 2.0E-36
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 1.000 13 3 2012 2017
Entrez Id: 2697
Gene Symbol: GJA1
GJA1
gap junction protein alpha 1 0.393 0.885 0.16
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 1.000 12 1 2003 2017
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
cyclin dependent kinase inhibitor 2A 0.300 0.885 0.39
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.100 None 1.000 8 1 2000 2011
Entrez Id: 28982
Gene Symbol: FLVCR1
FLVCR1
FLVCR heme transporter 1 0.529 0.885 1.3E-03
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.110 None 1.000 7 2 1997 2016
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
solute carrier family 6 member 3 0.453 0.885 1.00
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.070 None 1.000 7 0 2009 2019
Entrez Id: 1565
Gene Symbol: CYP2D6
CYP2D6
cytochrome P450 family 2 subfamily D member 6 0.437 0.885 1.1E-25
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.040 None 0.750 4 0 1997 2002
Entrez Id: 7054
Gene Symbol: TH
TH
tyrosine hydroxylase 0.462 0.885 1.7E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.110 None 1.000 4 1 2000 2014
Entrez Id: 2348
Gene Symbol: FOLR1
FOLR1
folate receptor alpha 0.522 0.885 0.13
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.310 None 1.000 2 0 2009 2019
Entrez Id: 1576
Gene Symbol: CYP3A4
CYP3A4
cytochrome P450 family 3 subfamily A member 4 0.462 0.885 5.8E-11
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 1728
Gene Symbol: NQO1
NQO1
NAD(P)H quinone dehydrogenase 1 0.434 0.885 1.2E-09
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.010 None 1.000 1 0 2012 2012
Entrez Id: 174
Gene Symbol: AFP
AFP
alpha fetoprotein 0.429 0.885 1.1E-11
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.010 None 1.000 1 0 2014 2014
Entrez Id: 2668
Gene Symbol: GDNF
GDNF
glial cell derived neurotrophic factor 0.434 0.885 0.20
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
group 0.010 None 1.000 1 0 2016 2016