TUBB4B

tubulin beta 4B class IVb
OMIM: 602660, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green TUBB4B in Ciliary Dyskinesia Level 2: Respiratory disorders Version 1.39	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Other Phenotypes Primary ciliary dyskinesia, MONDO:0016575, TUBB4B-related
Green TUBB4B in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Leber congenital amaurosis with early onset deafness, LCAEOD, OMIM #617879 MONDO:0060650 Primary ciliary dyskinesia, MONDO:0016575, TUBB4B-related
Green TUBB4B in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.194	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Leber congenital amaurosis with early-onset deafness, MIM# 617879
Green TUBB4B in Syndromic Retinopathy Level 2: Ophthalmological disorders Version 0.209 Component of the following Super Panels: Retinal Disorders Superpanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Green Expert list Victorian Clinical Genetics Services Phenotypes Leber congenital amaurosis with early-onset deafness MIM#617879 Primary ciliary dyskinesia, MONDO:0016575, TUBB4B-related
Green TUBB4B in Deafness_Isolated Level 2: Hearing and ear disorders Version 1.63	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Melbourne Genomics Health Alliance Deafness Flagship Phenotypes Leber congenital amaurosis with early-onset deafness
Red TUBB4B in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes Leber congenital amaurosis with early-onset deafness MIM#617879