AXIN2

axin 2
OMIM: 604025, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green AXIN2 in Mendeliome Version 2.305	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Oligodontia-colorectal cancer syndrome, MIM# 608615
Green AXIN2 in Oligodontia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Oligodontia-colorectal cancer syndrome, MIM# 608615
Amber AXIN2 in Ectodermal Dysplasia Level 2: Dermatological disorders Version 1.5	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert Review Phenotypes Oligodontia-colorectal cancer syndrome, MIM# 608615
No list AXIN2 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Phenotypes Oligodontia-colorectal cancer syndrome (MIM#608615)
No list AXIN2 in Choanal atresia Level 2: Dysmorphic and congenital abnormality syndromes Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Literature Phenotypes Oligodontia-colorectal cancer syndrome (MIM#608615)
Green AXIN2 in Colorectal Cancer and Polyposis Level 2: Cancer Predisposition Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes AXIN2-related attenuated familial adenomatous polyposis, MONDO:0018426 Oligodontia-cancer predisposition syndrome, MONDO:0012075 Oligodontia-colorectal cancer syndrome, MIM#608615