Gene: HCFC1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3054
Gene Symbol: HCFC1
HCFC1 		0.310 GermlineCausalMutation disease ORPHANET A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability. 23000143 2012
Entrez Id: 3054
Gene Symbol: HCFC1
HCFC1 		0.310 Biomarker disease BEFREE Non-specific mental retardations (MRX) are given unique symbols for each family (MRX1, MRX2, MRX3 ...). 1605216 1992