small embryonic telencephalon Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the paired diverticula of the embryonic telencephalon, from which the forebrain develops (Mammalian Phenotype Ontology, MP_0000936)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000936
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Genes

15 gene mutations causing the small embryonic telencephalon phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
FGF8 fibroblast growth factor 8 (androgen-induced)
FOXG1 forkhead box G1
HESX1 HESX homeobox 1
HHAT hedgehog acyltransferase
HHEX hematopoietically expressed homeobox
HSD17B7 hydroxysteroid (17-beta) dehydrogenase 7
LRP2 low density lipoprotein receptor-related protein 2
MECOM MDS1 and EVI1 complex locus
NUMB numb homolog (Drosophila)
PAX3 paired box 3
PGAP1 post-GPI attachment to proteins 1
PSEN1 presenilin 1
REST RE1-silencing transcription factor
TCTN1 tectonic family member 1