Gene: ARMC5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79798
Gene Symbol: ARMC5
ARMC5 		0.520 Biomarker disease BEFREE ARMC5 was the causative gene of AIMAH pedigrees. 29279458 2018
Entrez Id: 79798
Gene Symbol: ARMC5
ARMC5 		0.520 GeneticVariation disease BEFREE Some cases of corticotropin-independent macronodular adrenal hyperplasia appear to be genetic, most often with inactivating mutations of ARMC5, a putative tumor-suppressor gene. 24283224 2013
Entrez Id: 79798
Gene Symbol: ARMC5
ARMC5 		0.520 GermlineCausalMutation disease ORPHANET Some cases of corticotropin-independent macronodular adrenal hyperplasia appear to be genetic, most often with inactivating mutations of ARMC5, a putative tumor-suppressor gene. 24283224 2013
Entrez Id: 79798
Gene Symbol: ARMC5
ARMC5 		0.520 Biomarker disease CTD_human