CEACAM16

carcinoembryonic antigen related cell adhesion molecule 16
OMIM: 614591, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green CEACAM16 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal dominant 4B, MIM# 614614
  • Deafness, autosomal recessive 113, MIM# 618410

Green CEACAM16 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.194

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal dominant 4B, MIM# 614614
  • Deafness, autosomal recessive 113, MIM# 618410

Red CEACAM16 in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.63

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Expert Review Green
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal dominant 4B, MIM# 614614
  • Deafness, autosomal recessive 113, MIM# 618410

Red CEACAM16 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Hearing loss, autosomal dominant

Red CEACAM16 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Hearing loss, autosomal dominant