absent anterior commissure Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of a round bundle of nerve fibers that crosses the midline of the brain near the anterior limit of the third ventricle (Mammalian Phenotype Ontology, MP_0008227)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008227
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Genes

14 gene mutations causing the absent anterior commissure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARHGAP35 Rho GTPase activating protein 35
BHLHE22 basic helix-loop-helix family, member e22
CELSR3 cadherin, EGF LAG seven-pass G-type receptor 3
DRAXIN dorsal inhibitory axon guidance protein
EPHA4 EPH receptor A4
FBXO45 F-box protein 45
FZD3 frizzled class receptor 3
GLI3 GLI family zinc finger 3
HESX1 HESX homeobox 1
KLF7 Kruppel-like factor 7 (ubiquitous)
MAP3K12 mitogen-activated protein kinase kinase kinase 12
MYCBP2 MYC binding protein 2, E3 ubiquitin protein ligase
TMEM67 transmembrane protein 67
TUBB2B tubulin, beta 2B class IIb