MSX2

msh homeobox 2
OMIM: 123101, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green MSX2 in Craniosynostosis Level 2: Dysmorphic and congenital abnormality syndromes Version 1.68	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Craniosynostosis 2, MIM# 604757
Green MSX2 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Craniosynostosis 2 (MIM#604757) Parietal foramina 1 (MIM#168500) Parietal foramina with cleidocranial dysplasia (MIM#168550)
Green MSX2 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Illumina TruGenome Clinical Sequencing Services UKGTN Expert Review Green Radboud University Medical Center, Nijmegen NHS GMS Expert list Phenotypes Parietal foramina 1 168500 Parietal foramina with cleidocranial dysplasia 168550 Craniosynostosis, type 2 604757
Green MSX2 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Parietal foramina 1
Green MSX2 in Fetal anomalies Version 1.313	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Phenotypes Craniosynostosis 2 (MIM#604757) Parietal foramina 1 (MIM#168500) Parietal foramina with cleidocranial dysplasia (MIM#168550)
Red MSX2 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category A gene Phenotypes Craniosynostosis 2 (MIM#604757) Parietal foramina 1 (MIM#168500) Parietal foramina with cleidocranial dysplasia (MIM#168550)