abnormal primary somatosensory cortex morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the area of the postcentral gyrus and central sulcus that is involved in somatic sensation (Mammalian Phenotype Ontology, MP_0000860)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000860
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Genes

13 gene mutations causing the abnormal primary somatosensory cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY1 adenylate cyclase 1 (brain)
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
BDNF brain-derived neurotrophic factor
BHLHE22 basic helix-loop-helix family, member e22
EPHA4 EPH receptor A4
GAP43 growth associated protein 43
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
LEF1 lymphoid enhancer-binding factor 1
NR2F1 nuclear receptor subfamily 2, group F, member 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PLXNA4 plexin A4
RIMS1 regulating synaptic membrane exocytosis 1
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4