Gene symbol and protein | Gene Location | All allelic disease phenotypes - locus/disease symbols | |
AR Androgen receptor       | Xq11.2-q12 | * Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.49)* Kennedy disease - KD (12.49) | |
AR Androgen receptor | Xq11.2-q12 | * Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.49)* Kennedy disease - KD (12.49) | |
ARHGEF10 Rho guanine nucleotide exchange factor 10 | 8p23 | * Slowed nerve conduction velocity, autosomal dominant - NCV (14.13) | |
AR Androgen receptor | Xq11.2-q12 | * Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.49)* Kennedy disease - KD (12.49) | |
ARHGEF10 Rho guanine nucleotide exchange factor 10 | 8p23 | * Slowed nerve conduction velocity, autosomal dominant - NCV (14.13) | |
ARL6IP1 ADP-ribosylation factor-like 6 interacting protein 1 | 16p12.3 | * Spastic paraplegia 61, autosomal recessive - SPG61 (15.58) | |
AR Androgen receptor | Xq11.2-q12 | * Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.49)* Kennedy disease - KD (12.49) | |
ARHGEF10 Rho guanine nucleotide exchange factor 10 | 8p23 | * Slowed nerve conduction velocity, autosomal dominant - NCV (14.13) | |
ARL6IP1 ADP-ribosylation factor-like 6 interacting protein 1 | 16p12.3 | * Spastic paraplegia 61, autosomal recessive - SPG61 (15.58) | |
ARVD3? | | 14q12-q22 | * Arrhythmogenic right ventricular cardiomyopathy 3 - ARVC3 (10.117)* Arrhythmogenic right ventricular dysplasia-3 - ARVD3 (10.117) |
AR Androgen receptor | Xq11.2-q12 | * Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.49)* Kennedy disease - KD (12.49) | |
ARHGEF10 Rho guanine nucleotide exchange factor 10 | 8p23 | * Slowed nerve conduction velocity, autosomal dominant - NCV (14.13) | |
ARL6IP1 ADP-ribosylation factor-like 6 interacting protein 1 | 16p12.3 | * Spastic paraplegia 61, autosomal recessive - SPG61 (15.58) | |
ARVD3? | | 14q12-q22 | * Arrhythmogenic right ventricular cardiomyopathy 3 - ARVC3 (10.117)* Arrhythmogenic right ventricular dysplasia-3 - ARVD3 (10.117) |
ARVD4? | | 2q32.1-q32.3 | * Arrhythmogenic right ventricular cardiomyopathy 4 - ARVC4 (10.118)* Arrhythmogenic right ventricular dysplasia, familial, 4 - ARVD4 (10.118) |