absent forebrain Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the anterior of the three primary divisions of the developing chordate brain or the corresponding part of the adult brain (in vertebrates, includes especially the cerebral hemispheres, the thalamus, and the hypothalamus and especially in higher vertebrates is the main control center for sensory and associative information processing, visceral functions, and voluntary motor functions) (Mammalian Phenotype Ontology, MP_0012136)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012136
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Genes

13 gene mutations causing the absent forebrain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
AXIN1 axin 1
FOLR1 folate receptor 1 (adult)
HHEX hematopoietically expressed homeobox
LHX1 LIM homeobox 1
NODAL nodal growth differentiation factor
NPM1 nucleophosmin (nucleolar phosphoprotein B23, numatrin)
OTX2 orthodenticle homeobox 2
PDPK1 3-phosphoinositide dependent protein kinase 1
PTCH1 patched 1
RAX retina and anterior neural fold homeobox
SMAD5 SMAD family member 5
SSBP3 single stranded DNA binding protein 3