abnormal somatotroph morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of an acidophilic cell of the anterior pituitary that produces growth hormone, somatotropin (Mammalian Phenotype Ontology, MP_0008322)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008322
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Genes

19 gene mutations causing the abnormal somatotroph morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANXA1 annexin A1
CGA glycoprotein hormones, alpha polypeptide
CSHL1 chorionic somatomammotropin hormone-like 1
DMD dystrophin
DRD2 dopamine receptor D2
EGR1 early growth response 1
GHRHR growth hormone releasing hormone receptor
GSX1 GS homeobox 1
INSM1 insulinoma-associated 1
KL klotho
LHX3 LIM homeobox 3
PAX8 paired box 8
PITX2 paired-like homeodomain 2
POU1F1 POU class 1 homeobox 1
PROP1 PROP paired-like homeobox 1
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SOX2 SRY (sex determining region Y)-box 2
WNT4 wingless-type MMTV integration site family, member 4