delayed gross motor development Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of motor delay characterized by an delay in acquiring the ability to control the large muscles of the body for walking, running, sitting, and crawling. (Human Phenotype Ontology, HP_0002194)
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21 genes associated with the delayed gross motor development phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMP1 bone morphogenetic protein 1
CFL2 cofilin 2 (muscle)
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
CNTNAP2 contactin associated protein-like 2
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
DLAT dihydrolipoamide S-acetyltransferase
DSE dermatan sulfate epimerase
FGF3 fibroblast growth factor 3
FKRP fukutin related protein
FTSJ1 FtsJ RNA methyltransferase homolog 1 (E. coli)
GALE UDP-galactose-4-epimerase
HARS histidyl-tRNA synthetase
HOXA1 homeobox A1
NPHP1 nephronophthisis 1 (juvenile)
PAK3 p21 protein (Cdc42/Rac)-activated kinase 3
PTEN phosphatase and tensin homolog
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SUCLA2 succinate-CoA ligase, ADP-forming, beta subunit
TK2 thymidine kinase 2, mitochondrial
TNNT1 troponin T type 1 (skeletal, slow)