abnormal adrenal medulla morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the inner portion of the adrenal gland that consists mainly of chromaffin cells which produce, store and secrete neurotransmitters such as epinephrine and norepinephrine (Mammalian Phenotype Ontology, MP_0008289)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008289
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Genes

16 gene mutations causing the abnormal adrenal medulla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
APOE apolipoprotein E
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CHGB chromogranin B
CRHR1 corticotropin releasing hormone receptor 1
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
EGLN3 egl-9 family hypoxia-inducible factor 3
ERBB3 erb-b2 receptor tyrosine kinase 3
LEPR leptin receptor
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
RET ret proto-oncogene
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
SOX10 SRY (sex determining region Y)-box 10
STX1B syntaxin 1B
VAMP2 vesicle-associated membrane protein 2 (synaptobrevin 2)
VAV2 vav 2 guanine nucleotide exchange factor