abnormal adrenal gland physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the surparenal gland, including the ability to produce and secrete hormones (Mammalian Phenotype Ontology, MP_0002909)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002909
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Genes

25 gene mutations causing the abnormal adrenal gland physiology 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
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
DRD2 dopamine receptor D2
DRD5 dopamine receptor D5
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
SCARB1 scavenger receptor class B, member 1
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SNAPIN SNAP-associated protein
SYT1 synaptotagmin I
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TLR2 toll-like receptor 2
VAV2 vav 2 guanine nucleotide exchange factor
WNT4 wingless-type MMTV integration site family, member 4