DCC

DCC netrin 1 receptor
OMIM: 120470, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Red DCC in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.389	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Mirror movements 1 and/or agenesis of the corpus callosum, MIM#157600
Green DCC in Mendeliome Version 1.2302	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Phenotypes Mirror movements 1 and/or agenesis of the corpus callosum, OMIM #157600 Gaze palsy, familial horizontal, with progressive scoliosis, 2,OMIM # 617542
Green DCC in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.540	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Agenesis of the corpus callosum
Green DCC in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.302	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Literature NHS GMS Victorian Clinical Genetics Services Phenotypes Gaze palsy, familial horizontal, with progressive scoliosis, 2, MIM# 617542
Green DCC in Mirror movements Level 2: Neurology and neurodevelopmental disorders Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Mirror movements 1 and/or agenesis of the corpus callosum MIM#157600
Green DCC in Fetal anomalies Version 1.313	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Mirror movements 1 and/or agenesis of the corpus callosum, OMIM #157600 Gaze palsy, familial horizontal, with progressive scoliosis, 2,OMIM # 617542