developmental coordination disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A specific developmental disorder that involves disordered motor skills where coordinated muscle movement is impaired. (Human Disease Ontology, DOID_9923)
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24 genes co-occuring with the disease developmental coordination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ABCA2 ATP-binding cassette, sub-family A (ABC1), member 2 2.1582
MND1 meiotic nuclear divisions 1 homolog (S. cerevisiae) 1.85958
CHD6 chromodomain helicase DNA binding protein 6 1.47725
RBM8A RNA binding motif protein 8A 1.4022
ELP4 elongator acetyltransferase complex subunit 4 1.35681
MAP2K5 mitogen-activated protein kinase kinase 5 1.30969
AMY1B amylase, alpha 1B (salivary) 1.1422
AMY1A amylase, alpha 1A (salivary) 1.1422
AMY1C amylase, alpha 1C (salivary) 1.1422
KCNK6 potassium channel, two pore domain subfamily K, member 6 1.13332
PFN2 profilin 2 1.08076
DAD1 defender against cell death 1 1.05177
CUTA cutA divalent cation tolerance homolog (E. coli) 1.03662
FUT3 fucosyltransferase 3 (galactoside 3(4)-L-fucosyltransferase, Lewis blood group) 0.932484
BMP2K BMP2 inducible kinase 0.927105
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8 0.859362
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11 0.847488
NBPF10 neuroblastoma breakpoint family, member 10 0.733001
LY96 lymphocyte antigen 96 0.67551
GPANK1 G patch domain and ankyrin repeats 1 0.658818
CTSC cathepsin C 0.508808
CAMP cathelicidin antimicrobial peptide 0.507657
TH tyrosine hydroxylase 0.187113
RET ret proto-oncogene 0.167915