abnormal limb posture Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description atypical intentionally or habitually assumed position of the limbs compared to the normal carriage of the body (Mammalian Phenotype Ontology, MP_0004263)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004263
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20 gene mutations causing the abnormal limb posture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARAF A-Raf proto-oncogene, serine/threonine kinase
CDO1 cysteine dioxygenase type 1
CLCN1 chloride channel, voltage-sensitive 1
CNTNAP1 contactin associated protein 1
EGR3 early growth response 3
FIG4 FIG4 phosphoinositide 5-phosphatase
GRIA2 glutamate receptor, ionotropic, AMPA 2
LARGE like-glycosyltransferase
LRSAM1 leucine rich repeat and sterile alpha motif containing 1
MAP1B microtubule-associated protein 1B
MEOX2 mesenchyme homeobox 2
MYO5A myosin VA (heavy chain 12, myoxin)
NEUROG2 neurogenin 2
NTF3 neurotrophin 3
RND3 Rho family GTPase 3
RORA RAR-related orphan receptor A
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC6A9 solute carrier family 6 (neurotransmitter transporter, glycine), member 9
SOX10 SRY (sex determining region Y)-box 10
TCF15 transcription factor 15 (basic helix-loop-helix)