dilated third ventricle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An increase in size of the third ventricle. (Human Phenotype Ontology, HP_0007082)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000827
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Genes

27 gene mutations causing the dilated third ventricle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CELSR2 cadherin, EGF LAG seven-pass G-type receptor 2
CHD7 chromodomain helicase DNA binding protein 7
COL18A1 collagen, type XVIII, alpha 1
DHCR7 7-dehydrocholesterol reductase
DPCD deleted in primary ciliary dyskinesia homolog (mouse)
E2F5 E2F transcription factor 5, p130-binding
EMX2 empty spiracles homeobox 2
FZD3 frizzled class receptor 3
HSF1 heat shock transcription factor 1
HSF2 heat shock transcription factor 2
MBOAT7 membrane bound O-acyltransferase domain containing 7
MSX1 msh homeobox 1
MYH10 myosin, heavy chain 10, non-muscle
NAPA N-ethylmaleimide-sensitive factor attachment protein, alpha
NCOA6 nuclear receptor coactivator 6
NCOR1 nuclear receptor corepressor 1
NEK1 NIMA-related kinase 1
NFIA nuclear factor I/A
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NME7 NME/NM23 family member 7
OPHN1 oligophrenin 1
PFDN5 prefoldin subunit 5
PKD1 polycystic kidney disease 1 (autosomal dominant)
RND3 Rho family GTPase 3
SPAG6 sperm associated antigen 6
ULK4 unc-51 like kinase 4
ZIC5 Zic family member 5