abnormal hypothalamus secretion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered ability of the hypothalamus to produce or release biologically active substances (Mammalian Phenotype Ontology, MP_0001752)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001752
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Genes

10 gene mutations causing the abnormal hypothalamus secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CPE carboxypeptidase E
EBF2 early B-cell factor 2
FGF21 fibroblast growth factor 21
GSX1 GS homeobox 1
HMX2 H6 family homeobox 2
HMX3 H6 family homeobox 3
MAGEL2 melanoma antigen family L2
NOS1 nitric oxide synthase 1 (neuronal)
STX1A syntaxin 1A (brain)
Funding