prenatal movement abnormality Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of fetal movement. (Human Phenotype Ontology, HP_0001557)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001557
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Genes

74 genes associated with the prenatal movement abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
ASCL1 achaete-scute family bHLH transcription factor 1
BMP4 bone morphogenetic protein 4
CAMKMT calmodulin-lysine N-methyltransferase
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
FLII flightless I homolog (Drosophila)
GBA glucosidase, beta, acid
GBE1 glucan (1,4-alpha-), branching enzyme 1
GLE1 GLE1 RNA export mediator
GMPPB GDP-mannose pyrophosphorylase B
HDAC8 histone deacetylase 8
HSPG2 heparan sulfate proteoglycan 2
IGHMBP2 immunoglobulin mu binding protein 2
ISPD isoprenoid synthase domain containing
KIF5C kinesin family member 5C
KLHL41 kelch-like family member 41
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
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
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NDN necdin, melanoma antigen (MAGE) family member
NEB nebulin
NECAP1 NECAP endocytosis associated 1
NELFA negative elongation factor complex member A
NIPBL Nipped-B homolog (Drosophila)
PHGDH phosphoglycerate dehydrogenase
PHOX2B paired-like homeobox 2b
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
PPM1B protein phosphatase, Mg2+/Mn2+ dependent, 1B
PREPL prolyl endopeptidase-like
PSAT1 phosphoserine aminotransferase 1
RAD21 RAD21 homolog (S. pombe)
RAI1 retinoic acid induced 1
RAPSN receptor-associated protein of the synapse
RET ret proto-oncogene
RYR1 ryanodine receptor 1 (skeletal)
SEPN1 selenoprotein N, 1
SIX6 SIX homeobox 6
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
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
VPS13B vacuolar protein sorting 13 homolog B (yeast)
WDR62 WD repeat domain 62
WHSC1 Wolf-Hirschhorn syndrome candidate 1
ZC4H2 zinc finger, C4H2 domain containing
ZMPSTE24 zinc metallopeptidase STE24