CEACAM16

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

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green CEACAM16 in Mendeliome Version 1.3512	1 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 1.238	1 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 1.82	2 reviews	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	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Hearing loss, autosomal dominant
Red CEACAM16 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Hearing loss, autosomal dominant