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 (12.40)
* Kennedy disease - KD (12.40)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.40)
* Kennedy disease - KD (12.40)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.10)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.40)
* Kennedy disease - KD (12.40)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.10)
ARL6IP1
ADP-ribosylation factor-like 6 interacting protein 1




16p12.3
* Spastic paraplegia 61, autosomal recessive - SPG61 (15.57)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.40)
* Kennedy disease - KD (12.40)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.10)
ARL6IP1
ADP-ribosylation factor-like 6 interacting protein 1




16p12.3
* Spastic paraplegia 61, autosomal recessive - SPG61 (15.57)
ARVD3?

14q12-q22
* Arrhythmogenic right ventricular cardiomyopathy 3 - ARVC3 (10.105)
* Arrhythmogenic right ventricular dysplasia-3 - ARVD3 (10.105)
AR
Androgen receptor




Xq11.2-q12
* Spinal and bulbar muscular atrophy of Kennedy - SBMA (12.40)
* Kennedy disease - KD (12.40)
ARHGEF10
Rho guanine nucleotide exchange factor 10




8p23
* Slowed nerve conduction velocity, autosomal dominant - NCV (14.10)
ARL6IP1
ADP-ribosylation factor-like 6 interacting protein 1




16p12.3
* Spastic paraplegia 61, autosomal recessive - SPG61 (15.57)
ARVD3?

14q12-q22
* Arrhythmogenic right ventricular cardiomyopathy 3 - ARVC3 (10.105)
* Arrhythmogenic right ventricular dysplasia-3 - ARVD3 (10.105)
ARVD4?

2q32.1-q32.3
* Arrhythmogenic right ventricular cardiomyopathy 4 - ARVC4 (10.106)
* Arrhythmogenic right ventricular dysplasia, familial, 4 - ARVD4 (10.106)
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