Facial Paralysis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D005158
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Genes

25 genes/proteins associated with the disease Facial Paralysis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
POMC proopiomelanocortin 2.88009
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.40925
TNF tumor necrosis factor 1.37189
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.33995
F2 coagulation factor II (thrombin) 1.3231
BAX BCL2-associated X protein 1.27224
PRL prolactin 1.24118
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2 1.22306
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5 1.22145
RRM2 ribonucleotide reductase M2 1.21984
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.19379
RELA v-rel avian reticuloendotheliosis viral oncogene homolog A 1.18981
FAS Fas cell surface death receptor 1.14268
PARP1 poly (ADP-ribose) polymerase 1 1.12082
TNFSF10 tumor necrosis factor (ligand) superfamily, member 10 1.10246
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) 1.09646
CTSL cathepsin L 1.09083
CCL2 chemokine (C-C motif) ligand 2 1.07589
ATF3 activating transcription factor 3 1.07376
CXCL8 chemokine (C-X-C motif) ligand 8 1.07163
IL10 interleukin 10 1.06225
ABCC1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 1.05864
NR1I2 nuclear receptor subfamily 1, group I, member 2 1.05793
CASP8 caspase 8, apoptosis-related cysteine peptidase 1.02708
VCAM1 vascular cell adhesion molecule 1 1.01174