GT/TP identifiers for the NHSE Digital Genomic Test Service are temporarily visible in PanelApp but are not yet in use in Genomics England systems

DNM1

dynamin 1
OMIM: 602377, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber DNM1 in Fetal anomalies Level 2: Fetal (including NIPD) Version 7.33 Latest signed off version: v7.0 (6 May 2026)	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber PAGE DD-Gene2Phenotype Phenotypes EPILEPTIC ENCEPHALOPATHY
Green DNM1 in DDG2P Version 7.8 Latest signed off version: v7.0 (6 May 2026) Component of the following Super Panels: Paediatric disorders	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green DD-Gene2Phenotype Phenotypes EPILEPTIC ENCEPHALOPATHY
Green DNM1 in Early onset or syndromic epilepsy Level 2: Neurology Version 9.53 Latest signed off version: v9.0 (6 May 2026) Component of the following Super Panels: Paediatric disorders Unexplained death in infancy and sudden unexplained death in childhood	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Wessex and West Midlands GLH NHS GMS Victorian Clinical Genetics Services Expert Review Phenotypes Developmental and epileptic encephalopathy 31B, autosomal recessive, OMIM:620352 developmental and epileptic encephalopathy, 31B, MONDO:0957248 Developmental and epileptic encephalopathy 31A, autosomal dominant, OMIM:616346 developmental and epileptic encephalopathy, 31A, MONDO:0014598 DNM1 early infantile epileptic encephalopathy Tags Q3_26_MOI
Green DNM1 in Intellectual disability Level 2: Developmental disorders Version 10.83 Latest signed off version: v10.0 (6 May 2026) Component of the following Super Panels: Childhood onset leukodystrophy Hypotonic infant Paediatric disorders	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Developmental and epileptic encephalopathy 31B, autosomal recessive, OMIM:620352 developmental and epileptic encephalopathy, 31B, MONDO:0957248 Developmental and epileptic encephalopathy 31A, autosomal dominant, OMIM:616346 developmental and epileptic encephalopathy, 31A, MONDO:0014598 DNM1 early infantile epileptic encephalopathy Tags Q3_26_MOI