Gait Ataxia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of ataxia characterized by the impairment of the ability to coordinate the movements required for normal walking. Gait ataxia is characteirzed by a wide-based staggering gait with a tendency to fall. (Human Phenotype Ontology, HP_0002066)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D020234
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Genes

13 genes/proteins associated with the disease Gait Ataxia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.55084
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.27905
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2 1.2596
ABCC1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 1.2013
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.17926
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2 1.1529
ABCC3 ATP-binding cassette, sub-family C (CFTR/MRP), member 3 1.11843
BCL2 B-cell CLL/lymphoma 2 1.08797
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2 1.07553
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1) 1.07234
S100A8 S100 calcium binding protein A8 1.05535
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9 1.05015
NR1I2 nuclear receptor subfamily 1, group I, member 2 1.04389