Pheochromocytoma Gene Set
Dataset
CTD Gene-Disease Associations
Category
disease or phenotype associations
Type
disease
Description
Pheochromocytomas (also known as chromaffin tumors) produce, store, and secrete catecholamines. Pheochromocytomas usually originate from the adrenal medulla but may also develop from chromaffin cells in or about sympathetic ganglia. A common symptom of pheochromocytoma is hypertension owing to release of catecholamines. (Human Phenotype Ontology , HP_0002666 )
External Link
http://ctdbase.org/detail.go?type=disease&acc=MESH:D010673
Similar Terms
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Genes
18 genes/proteins associated with the disease Pheochromocytoma from the curated CTD Gene-Disease Associations dataset.
Symbol
Name
Standardized Value
DDC
dopa decarboxylase (aromatic L-amino acid decarboxylase)
2.88009
MAX
MYC associated factor X
2.88009
NF1
neurofibromin 1
2.88009
GDNF
glial cell derived neurotrophic factor
2.88009
CHGA
chromogranin A
2.88009
RET
ret proto-oncogene
2.88009
TMEM127
transmembrane protein 127
2.88009
DBH
dopamine beta-hydroxylase (dopamine beta-monooxygenase)
2.88009
KIF1B
kinesin family member 1B
2.88009
SDHD
succinate dehydrogenase complex, subunit D, integral membrane protein
2.88009
SDHB
succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
2.88009
VHL
von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
2.88009
COMT
catechol-O-methyltransferase
2.88009
MAOA
monoamine oxidase A
2.88009
MAOB
monoamine oxidase B
2.88009
TH
tyrosine hydroxylase
2.88009
SLC22A2
solute carrier family 22 (organic cation transporter), member 2
1.0766
SLC22A3
solute carrier family 22 (organic cation transporter), member 3
1.04389
