impaired limb coordination Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced ability to organize limb movements to execute complex maneuvers, such as walking (Mammalian Phenotype Ontology, MP_0001524)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001524
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Genes

50 gene mutations causing the impaired limb coordination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRG6 adhesion G protein-coupled receptor G6
AGA aspartylglucosaminidase
AGRN agrin
ATF2 activating transcription factor 2
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
BDNF brain-derived neurotrophic factor
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CDK4 cyclin-dependent kinase 4
CLCN1 chloride channel, voltage-sensitive 1
CNTN1 contactin 1
CNTNAP1 contactin associated protein 1
CYCS cytochrome c, somatic
DNM1 dynamin 1
DST dystonin
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
EFNB3 ephrin-B3
EGR2 early growth response 2
EPHA4 EPH receptor A4
ETV1 ets variant 1
ETV4 ets variant 4
GAL3ST1 galactose-3-O-sulfotransferase 1
GALC galactosylceramidase
GARS glycyl-tRNA synthetase
GLI2 GLI family zinc finger 2
GRM1 glutamate receptor, metabotropic 1
HTT huntingtin
KCNN2 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2
L1CAM L1 cell adhesion molecule
LAMA4 laminin, alpha 4
LDB3 LIM domain binding 3
LOC102723475 putative uncharacterized protein LOC388820
LPIN1 lipin 1
MID1 midline 1
MYO5A myosin VA (heavy chain 12, myoxin)
NTF3 neurotrophin 3
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
PARK7 parkinson protein 7
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PSAP prosaposin
RORA RAR-related orphan receptor A
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SHC1 SHC (Src homology 2 domain containing) transforming protein 1
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TRPC3 transient receptor potential cation channel, subfamily C, member 3
VAMP1 vesicle-associated membrane protein 1 (synaptobrevin 1)
ZIC1 Zic family member 1