INSL3

insulin like 3
OMIM: 146738, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber INSL3 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.44

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Cryptorchidism, MIM# 219050

Green INSL3 in Mendeliome


Version 1.4541

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Cryptorchidism, MIM# 219050
  • Infertility disorder MONDO:0005047, INSL3-related

Amber INSL3 in Primary Ovarian Insufficiency_Premature Ovarian Failure

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 0.404

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Primary ovarian insufficiency

Green INSL3 in Infertility and Recurrent Pregnancy Loss


Version 1.127

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • Victorian Clinical Genetics Services
Phenotypes
  • Cryptorchidism, MIM# 219050
  • Infertility disorder MONDO:0005047, INSL3-related