AR

androgen receptor
OMIM: 313700, ClinGen, DECIPHER

8 panels

Panel Reviews Mode of inheritance Details
8 panels

Green AR in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypospadias 1, X-linked MIM#30063
  • Androgen insensitivity MIM#300068
  • Androgen insensitivity, partial, with or without breast cancer MIM#312300

Green AR in Mendeliome


Version 2.0

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypospadias 1, X-linked MIM#30063
  • Androgen insensitivity MIM#300068
  • Androgen insensitivity, partial, with or without breast cancer MIM#312300
  • Spinal and bulbar muscular atrophy of Kennedy MIM#313200

Red AR in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Spinal and bulbar muscular atrophy of Kennedy, MIM# 313200

Green AR in Additional findings_Paediatric


Level 2: Screening
Version 1.0

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • BabySeq Category C gene
  • BabySeq Category A gene
Phenotypes
  • Androgen insensitivity, MIM# 300068

Green AR in Fetal anomalies


Version 2.0

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Genetic Health Queensland
Phenotypes
  • Androgen insensitivity, MIM# 300068
  • Androgen insensitivity syndrome, MONDO:0019154

Red AR in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • BabySeq Category C gene
  • BabySeq Category A gene
Phenotypes
  • Hypospadias 1, X-linked MIM#30063
  • Androgen insensitivity MIM#300068
  • Androgen insensitivity, partial, with or without breast cancer MIM#312300

Green AR_SBMA_CAG STR in Motor Neurone Disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Spinal and bulbar muscular atrophy of Kennedy MIM#313200
Tags
  • STR

Green AR_SBMA_CAG STR in Repeat Disorders


Version 1.0

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Spinal and bulbar muscular atrophy of Kennedy MIM#313200
Tags
  • adult-onset