abnormal adrenal chromaffin cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the neuroendocrine cells of the medulla of the adrenal gland that are innervated by the splanchnic nerve and that are responsible for epinephrine and norepinephrine secretion (Mammalian Phenotype Ontology, MP_0008504)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008504
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9 gene mutations causing the abnormal adrenal chromaffin cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHGB chromogranin B
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
EGLN3 egl-9 family hypoxia-inducible factor 3
ERBB3 erb-b2 receptor tyrosine kinase 3
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
STX1B syntaxin 1B
VAMP2 vesicle-associated membrane protein 2 (synaptobrevin 2)