decreased corpus callosum size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description smaller thick bundle of nerve fibers comprising a commissural plate connecting the two cerebral hemispheres; it consists of contralateral axon projections that provides communications between the right and left cerebral hemispheres (Mammalian Phenotype Ontology, MP_0000781)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000781
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Genes

29 gene mutations causing the decreased corpus callosum size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKT3 v-akt murine thymoma viral oncogene homolog 3
ANK2 ankyrin 2, neuronal
AP4E1 adaptor-related protein complex 4, epsilon 1 subunit
APP amyloid beta (A4) precursor protein
ARHGAP5 Rho GTPase activating protein 5
CDK5R1 cyclin-dependent kinase 5, regulatory subunit 1 (p35)
CLIP2 CAP-GLY domain containing linker protein 2
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
DRAXIN dorsal inhibitory axon guidance protein
EIF4H eukaryotic translation initiation factor 4H
EMX2 empty spiracles homeobox 2
FYN FYN proto-oncogene, Src family tyrosine kinase
FZD3 frizzled class receptor 3
GFAP glial fibrillary acidic protein
MAP1B microtubule-associated protein 1B
MAP3K12 mitogen-activated protein kinase kinase kinase 12
MYCBP2 MYC binding protein 2, E3 ubiquitin protein ligase
NIPBL Nipped-B homolog (Drosophila)
NPC1 Niemann-Pick disease, type C1
PFDN1 prefoldin subunit 1
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
RPGRIP1L RPGRIP1-like
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SOX2 SRY (sex determining region Y)-box 2
SUZ12 SUZ12 polycomb repressive complex 2 subunit
ULK4 unc-51 like kinase 4
USP14 ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)
WASF1 WAS protein family, member 1
ZIC2 Zic family member 2