enlarged third ventricle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased size of the narrow cleft inferior to the corpus callosum, within the diencephalon, between the paired thalami; its floor is formed by the hypothalamus, its anterior wall by the lamina terminalis, and its roof by ependyma; it communicates with the fourth ventricle by the cerebral aqueduct, and with the lateral ventricles by the interventricular foramina (Mammalian Phenotype Ontology, MP_0008536)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008536
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16 gene mutations causing the enlarged third ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
ARX aristaless related homeobox
ATP1B2 ATPase, Na+/K+ transporting, beta 2 polypeptide
ATXN1L ataxin 1-like
BBS1 Bardet-Biedl syndrome 1
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
HSF2 heat shock transcription factor 2
HTT huntingtin
MAP1B microtubule-associated protein 1B
MKKS McKusick-Kaufman syndrome
NPAS3 neuronal PAS domain protein 3
SLC17A6 solute carrier family 17 (vesicular glutamate transporter), member 6
SOX2 SRY (sex determining region Y)-box 2
USP18 ubiquitin specific peptidase 18
VANGL2 VANGL planar cell polarity protein 2