telencephalon hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, in of the enlarged anteriolateral part of the brain; consists of the paired cerebral hemispheres and olfactory bulbs, the basal ganglia and the connecting structures (Mammalian Phenotype Ontology, MP_0000785)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000785
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Genes

8 gene mutations causing the telencephalon hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
B9D1 B9 protein domain 1
DMRTA2 DMRT-like family A2
ID4 inhibitor of DNA binding 4, dominant negative helix-loop-helix protein
INTU inturned planar cell polarity protein
LIAS lipoic acid synthetase
MDM4 MDM4, p53 regulator
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
PAX6 paired box 6