MNX1

motor neuron and pancreas homeobox 1
OMIM: 142994, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green MNX1 in Skeletal Dysplasia_Fetal Level 2: Skeletal disorders Version 0.239	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Currarino syndrome, MIM# 176450
Green MNX1 in Mendeliome Version 1.3512	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Currarino syndrome, MIM# 176450 Permanent neonatal diabetes mellitus, MONDO:0100164, MNX1-related
Red MNX1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes Currarino syndrome OMIM #176450
Green MNX1 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.346	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Radboud University Medical Center, Nijmegen NHS GMS Phenotypes Currarino syndrome 176450
Green MNX1 in Monogenic Diabetes Level 2: Endocrine disorders Version 0.152 Component of the following Super Panels: Metabolic Disorders Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green UKGTN Phenotypes Permanent neonatal diabetes mellitus, MONDO:0100164, MNX1-related
Green MNX1 in Fetal anomalies Version 1.465	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Expert list Phenotypes Currarino syndrome, MIM# 176450
Green MNX1 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Permanent neonatal diabetes mellitus, MONDO:0100164, MNX1-related Tags treatable endocrine