abnormal neuroendocrine cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a neuron that has the specialized function to produce and secrete hormones, contains neruosecretory granules, and that constitutes, in whole or in part, an endocrine organ or system (Mammalian Phenotype Ontology, MP_0010913)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010913
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Genes

15 gene mutations causing the abnormal neuroendocrine cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASCL1 achaete-scute family bHLH transcription factor 1
CHGB chromogranin B
CRH corticotropin releasing hormone
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
EGLN3 egl-9 family hypoxia-inducible factor 3
ERBB3 erb-b2 receptor tyrosine kinase 3
FBN1 fibrillin 1
HES1 hes family bHLH transcription factor 1
NEUROD1 neuronal differentiation 1
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
RET ret proto-oncogene
SIM1 single-minded family bHLH transcription factor 1
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
STX1B syntaxin 1B
VAMP2 vesicle-associated membrane protein 2 (synaptobrevin 2)