abnormal parietal lobe morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the upper central part of the cerebral hemisphere (Mammalian Phenotype Ontology, MP_0000794)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000794
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Genes

26 gene mutations causing the abnormal parietal lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY1 adenylate cyclase 1 (brain)
ARHGAP33 Rho GTPase activating protein 33
ARX aristaless related homeobox
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
ATP7B ATPase, Cu++ transporting, beta polypeptide
BDNF brain-derived neurotrophic factor
BHLHE22 basic helix-loop-helix family, member e22
BRAF B-Raf proto-oncogene, serine/threonine kinase
CHD7 chromodomain helicase DNA binding protein 7
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
EPHA4 EPH receptor A4
ESR2 estrogen receptor 2 (ER beta)
FYN FYN proto-oncogene, Src family tyrosine kinase
GAP43 growth associated protein 43
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
LEF1 lymphoid enhancer-binding factor 1
MAP1B microtubule-associated protein 1B
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
MAPT microtubule-associated protein tau
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
TUBA1A tubulin, alpha 1a