abnormal pituitary gland development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description malformation or incomplete differentiation of the compound gland suspended from the base of the hypothalamus, which secretes somatotropins, prolactin, TSH (thyroid-stimulating hormone), gonadotropins, adrenal corticotropin (Mammalian Phenotype Ontology, MP_0003816)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003816
Similar Terms
Downloads & Tools

Genes

26 gene mutations causing the abnormal pituitary gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AES amino-terminal enhancer of split
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1
BMP4 bone morphogenetic protein 4
CHD7 chromodomain helicase DNA binding protein 7
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FOXC1 forkhead box C1
FUZ fuzzy planar cell polarity protein
HES1 hes family bHLH transcription factor 1
HESX1 HESX homeobox 1
HHEX hematopoietically expressed homeobox
INSM1 insulinoma-associated 1
ISL1 ISL LIM homeobox 1
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
NBEA neurobeachin
NKX2-1 NK2 homeobox 1
NOG noggin
PGAP1 post-GPI attachment to proteins 1
PITX2 paired-like homeodomain 2
PROP1 PROP paired-like homeobox 1
RPGRIP1L RPGRIP1-like
SOX2 SRY (sex determining region Y)-box 2
SOX3 SRY (sex determining region Y)-box 3
TCOF1 Treacher Collins-Franceschetti syndrome 1
TRH thyrotropin-releasing hormone