abnormal rathke's pouch development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the formation of the pouch of ectoderm which grows out from the upper surface of the embryonic stomodeum and gives rise to the anterior and intermediate lobes of the pituitary gland (Mammalian Phenotype Ontology, MP_0013351)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013351
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Genes

10 gene mutations causing the abnormal rathke's pouch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2
HESX1 HESX homeobox 1
ISL1 ISL LIM homeobox 1
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
NKX2-1 NK2 homeobox 1
NOG noggin
PITX2 paired-like homeodomain 2
SOX3 SRY (sex determining region Y)-box 3
TCOF1 Treacher Collins-Franceschetti syndrome 1