Cerebral Palsy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A brain disease that is caused by damage to the motor control centers of the developing brain during pregnancy, during childbirth or after birth, which affects muscle movement and balance. (Human Disease Ontology, DOID_1969)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D002547
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Genes

30 genes/proteins associated with the disease Cerebral Palsy from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
POMC proopiomelanocortin 2.88009
SOD1 superoxide dismutase 1, soluble 1.29133
CAT catalase 1.25245
IFNG interferon, gamma 1.18816
IL1B interleukin 1, beta 1.18816
IL4 interleukin 4 1.18391
CXCL8 chemokine (C-X-C motif) ligand 8 1.16104
IL6 interleukin 6 1.16104
TNF tumor necrosis factor 1.14954
BDNF brain-derived neurotrophic factor 1.13109
TP53 tumor protein p53 1.12048
HMOX1 heme oxygenase 1 1.1198
IGF2 insulin-like growth factor 2 1.10317
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1 1.09401
GSTM3 glutathione S-transferase mu 3 (brain) 1.0784
APP amyloid beta (A4) precursor protein 1.06844
SOD2 superoxide dismutase 2, mitochondrial 1.06661
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.0561
MT2A metallothionein 2A 1.04611
IGF1 insulin-like growth factor 1 (somatomedin C) 1.04501
CALCA calcitonin-related polypeptide alpha 1.03752
MAPK3 mitogen-activated protein kinase 3 1.03567
NGF nerve growth factor (beta polypeptide) 1.03084
MAPK1 mitogen-activated protein kinase 1 1.02821
NOS3 nitric oxide synthase 3 (endothelial cell) 1.02821
FOS FBJ murine osteosarcoma viral oncogene homolog 1.02596
GJA1 gap junction protein, alpha 1, 43kDa 1.01701
GSR glutathione reductase 1.01701
VIM vimentin 1.01512
CFB complement factor B 1.01512