absent corpus callosum Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the corpus callosum as a result of the failure of the corpus callosum to develop, which can be the result of a failure in any one of the multiple steps of callosal development including cellular proliferation and migration, axonal growth or glial patterning at the midline. (Human Phenotype Ontology, HP_0001274)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002196
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32 gene mutations causing the absent corpus callosum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKT3 v-akt murine thymoma viral oncogene homolog 3
APP amyloid beta (A4) precursor protein
ARHGAP35 Rho GTPase activating protein 35
ATR ATR serine/threonine kinase
BHLHE22 basic helix-loop-helix family, member e22
CABLES1 Cdk5 and Abl enzyme substrate 1
CASP9 caspase 9, apoptosis-related cysteine peptidase
CHD7 chromodomain helicase DNA binding protein 7
DCC DCC netrin 1 receptor
DCLK1 doublecortin-like kinase 1
DRAXIN dorsal inhibitory axon guidance protein
EFNB1 ephrin-B1
EMX1 empty spiracles homeobox 1
ENAH enabled homolog (Drosophila)
FEZF2 FEZ family zinc finger 2
FOXC1 forkhead box C1
GLI3 GLI family zinc finger 3
HESX1 HESX homeobox 1
LRP2 low density lipoprotein receptor-related protein 2
MAP1B microtubule-associated protein 1B
NFIA nuclear factor I/A
NFIB nuclear factor I/B
NIPBL Nipped-B homolog (Drosophila)
NTN1 netrin 1
PRDM8 PR domain containing 8
TUBB2B tubulin, beta 2B class IIb
TUBB3 tubulin, beta 3 class III
VAX1 ventral anterior homeobox 1
WDR47 WD repeat domain 47
ZNF423 zinc finger protein 423