abnormal adrenal gland secretion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered ability of the surparenal gland to produce or secrete hormones (Mammalian Phenotype Ontology, MP_0001739)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001739
Similar Terms
Downloads & Tools


20 gene mutations causing the abnormal adrenal gland secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANXA1 annexin A1
APOE apolipoprotein E
CADPS Ca++-dependent secretion activator
CHGA chromogranin A
CHGB chromogranin B
DRD2 dopamine receptor D2
EGLN3 egl-9 family hypoxia-inducible factor 3
FOXA1 forkhead box A1
ITSN1 intersectin 1 (SH3 domain protein)
LEP leptin
LRRK2 leucine-rich repeat kinase 2
LY6E lymphocyte antigen 6 complex, locus E
PLA2G10 phospholipase A2, group X
RCAN1 regulator of calcineurin 1
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SNAPIN SNAP-associated protein
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TLR2 toll-like receptor 2
VAV2 vav 2 guanine nucleotide exchange factor