small adrenal glands Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Developmental hypoplasia of the adrenal glands. (Human Phenotype Ontology, HP_0000835)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002768
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Genes

15 gene mutations causing the small adrenal glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
AVPR1B arginine vasopressin receptor 1B
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1
CRHR1 corticotropin releasing hormone receptor 1
CXCR2 chemokine (C-X-C motif) receptor 2
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
FOXD1 forkhead box D1
HMGA2 high mobility group AT-hook 2
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NR5A1 nuclear receptor subfamily 5, group A, member 1
PBX1 pre-B-cell leukemia homeobox 1
POMC proopiomelanocortin
SERP1 stress-associated endoplasmic reticulum protein 1
TBX19 T-box 19