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 (12.65)
* Kennedy disease - KD (12.65)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.65)
* Kennedy disease - KD (12.65)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.9)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.65)
* Kennedy disease - KD (12.65)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.9)
ARL6IP1
ADP-ribosylation factor-like 6 interacting protein 1




16p12.3
* Spastic paraplegia 61, autosomal recessive - SPG61 (15.53)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.65)
* Kennedy disease - KD (12.65)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.9)
ARL6IP1
ADP-ribosylation factor-like 6 interacting protein 1




16p12.3
* Spastic paraplegia 61, autosomal recessive - SPG61 (15.53)
ARVD3?

14q12-q22
* Arrhythmogenic right ventricular cardiomyopathy 3 - ARVC3 (10.81)
* Arrhythmogenic right ventricular dysplasia-3 - ARVD3 (10.81)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.65)
* Kennedy disease - KD (12.65)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.9)
ARL6IP1
ADP-ribosylation factor-like 6 interacting protein 1




16p12.3
* Spastic paraplegia 61, autosomal recessive - SPG61 (15.53)
ARVD3?

14q12-q22
* Arrhythmogenic right ventricular cardiomyopathy 3 - ARVC3 (10.81)
* Arrhythmogenic right ventricular dysplasia-3 - ARVD3 (10.81)
ARVD4?

2q32.1-q32.3
* Arrhythmogenic right ventricular cardiomyopathy 4 - ARVC4 (10.82)
* Arrhythmogenic right ventricular dysplasia, familial, 4 - ARVD4 (10.82)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.65)
* Kennedy disease - KD (12.65)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.9)
ARL6IP1
ADP-ribosylation factor-like 6 interacting protein 1




16p12.3
* Spastic paraplegia 61, autosomal recessive - SPG61 (15.53)
ARVD3?

14q12-q22
* Arrhythmogenic right ventricular cardiomyopathy 3 - ARVC3 (10.81)
* Arrhythmogenic right ventricular dysplasia-3 - ARVD3 (10.81)
ARVD4?

2q32.1-q32.3
* Arrhythmogenic right ventricular cardiomyopathy 4 - ARVC4 (10.82)
* Arrhythmogenic right ventricular dysplasia, familial, 4 - ARVD4 (10.82)
ARVD6?

10p14-p12
* Arrhythmogenic right ventricular dysplasia, familial, 6 - ARVD6 (10.84)
* Arrhythmogenic right ventricular cardiomyopathy 6 - ARVC6 (10.84)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.65)
* Kennedy disease - KD (12.65)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.9)
ARL6IP1
ADP-ribosylation factor-like 6 interacting protein 1




16p12.3
* Spastic paraplegia 61, autosomal recessive - SPG61 (15.53)
ARVD3?

14q12-q22
* Arrhythmogenic right ventricular cardiomyopathy 3 - ARVC3 (10.81)
* Arrhythmogenic right ventricular dysplasia-3 - ARVD3 (10.81)
ARVD4?

2q32.1-q32.3
* Arrhythmogenic right ventricular cardiomyopathy 4 - ARVC4 (10.82)
* Arrhythmogenic right ventricular dysplasia, familial, 4 - ARVD4 (10.82)
ARVD6?

10p14-p12
* Arrhythmogenic right ventricular dysplasia, familial, 6 - ARVD6 (10.84)
* Arrhythmogenic right ventricular cardiomyopathy 6 - ARVC6 (10.84)
ARVD7?

10q22.3
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