decreased fetal movement Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal reduction in quantity or strength of fetal movements. (Human Phenotype Ontology, HP_0001558)
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49 genes associated with the decreased fetal movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRNB1 cholinergic receptor, nicotinic, beta 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNE cholinergic receptor, nicotinic, epsilon (muscle)
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CNTN1 contactin 1
COL6A1 collagen, type VI, alpha 1
COL6A2 collagen, type VI, alpha 2
COL6A3 collagen, type VI, alpha 3
COX15 cytochrome c oxidase assembly homolog 15 (yeast)
DHCR7 7-dehydrocholesterol reductase
DMPK dystrophia myotonica-protein kinase
DNM1L dynamin 1-like
DNM2 dynamin 2
DOK7 docking protein 7
ERBB3 erb-b2 receptor tyrosine kinase 3
FGFR3 fibroblast growth factor receptor 3
GBA glucosidase, beta, acid
GBE1 glucan (1,4-alpha-), branching enzyme 1
GLE1 GLE1 RNA export mediator
GMPPB GDP-mannose pyrophosphorylase B
IGHMBP2 immunoglobulin mu binding protein 2
ISPD isoprenoid synthase domain containing
KIF5C kinesin family member 5C
KLHL41 kelch-like family member 41
LMNA lamin A/C
MEGF10 multiple EGF-like-domains 10
MTM1 myotubularin 1
MUSK muscle, skeletal, receptor tyrosine kinase
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NDN necdin, melanoma antigen (MAGE) family member
NEB nebulin
NECAP1 NECAP endocytosis associated 1
PHGDH phosphoglycerate dehydrogenase
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
RAPSN receptor-associated protein of the synapse
RYR1 ryanodine receptor 1 (skeletal)
SEPN1 selenoprotein N, 1
SMN1 survival of motor neuron 1, telomeric
SNRPN small nuclear ribonucleoprotein polypeptide N
TMCO1 transmembrane and coiled-coil domains 1
TPM3 tropomyosin 3
TRPV4 transient receptor potential cation channel, subfamily V, member 4
TSFM Ts translation elongation factor, mitochondrial
UBA1 ubiquitin-like modifier activating enzyme 1
WDR62 WD repeat domain 62
ZC4H2 zinc finger, C4H2 domain containing
ZMPSTE24 zinc metallopeptidase STE24