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Alagille syndrome
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Alternating Hemiplegia and Hemiplegic Migraine
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Amelogenesis imperfecta
Amelogenesis imperfecta
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Angelman Rett like syndromes
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Arrhythmogenic Cardiomyopathy
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Ataxia - adult onset
Ataxia_Superpanel
Atrial Fibrillation
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Atypical Haemolytic Uraemic Syndrome_MPGN
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Systemic Autoinflammatory Disease_Periodic Fever
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Bardet Biedl syndrome
Bardet Biedl syndrome
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Brugada syndrome
Brugada syndrome
Calcium and Phosphate disorders
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Callosome
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Cancer Predisposition_Paediatric
Cancer Predisposition_Paediatric
Cardiomyopathy_Adult_SuperPanel
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Cardiomyopathy_Paediatric
Cataract
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Catecholaminergic Polymorphic Ventricular Tachycardia
Central Hypoventilation
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Cerebellar and Pontocerebellar Hypoplasia
Cerebellar and Pontocerebellar Hypoplasia
Cerebral amyloid angiopathy
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Cerebral Palsy
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CGC_86
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Choanal atresia
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Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic
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Cutis Laxa
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IBMDx study
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Leukodystrophy - paediatric
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Limb-Girdle Muscular Dystrophy and Distal Myopathy
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Liverome Superpanel
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Mackenzie's Mission_Reproductive Carrier Screening
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Malignant Hyperthermia Susceptibility
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Mandibulofacial Acrofacial dysostosis
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Maturity-onset Diabetes of the Young
Medulloblastoma
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Melanoma
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Mendelian susceptibility to Immune Disorders
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Metabolic Disorders Superpanel
Metal Metabolism Disorders
Metal Metabolism Disorders
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Metaphyseal dysplasias
Microcephalic Primordial Dwarfism and Slender bone dysplasias
Microcephalic Primordial Dwarfism and Slender bone dysplasias
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Mirror movements
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Miscellaneous Metabolic Disorders
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Monogenic Diabetes
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Mosaic skin disorders
Motor Neurone Disease
Motor Neurone Disease
Multiple epiphyseal dysplasia and pseudoachondroplasia
Multiple epiphyseal dysplasia and pseudoachondroplasia
Multiple joint dislocations and laxity
Multiple joint dislocations and laxity
Multiple pterygium syndrome_Fetal akinesia sequence
Multiple pterygium syndrome_Fetal akinesia sequence
Muscular dystrophy and myopathy_Paediatric
Muscular dystrophy and myopathy_Paediatric
Myopathy Superpanel
NCGC
NCGC
Neurodegeneration with brain iron accumulation
Neurodegeneration with brain iron accumulation
Neurodegenerative disease - adult onset
Neuromuscular Superpanel
Neurotransmitter Defects
Neurotransmitter Defects
Nucleotide metabolism disorders
Nucleotide metabolism disorders
Ocular and Oculocutaneous Albinism
Ocular and Oculocutaneous Albinism
Oligodontia
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Optic Atrophy
Optic Atrophy
Osteogenesis Imperfecta and Osteoporosis
Osteogenesis Imperfecta and Osteoporosis
Osteopetrosis
Osteopetrosis
Overgrowth
Overgrowth
Pain syndromes
Pain syndromes
Palmoplantar Keratoderma and Erythrokeratoderma
Palmoplantar Keratoderma and Erythrokeratoderma
Pancreatitis
Pancreatitis
Paroxysmal Dyskinesia
Paroxysmal Dyskinesia
Periventricular Grey Matter Heterotopia
Periventricular Grey Matter Heterotopia
Peroxisomal Disorders
Peroxisomal Disorders
Phagocyte Defects
Phagocyte Defects
Pharmacogenomics_Paediatric
Pharmacogenomics_Paediatric
Photosensitivity Syndromes
Photosensitivity Syndromes
Pierre Robin Sequence
Pierre Robin Sequence
Pituitary hormone deficiency
Pituitary hormone deficiency
Pneumothorax
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Polycystic liver disease
Polycystic liver disease
Polydactyly
Polydactyly
Polymicrogyria and Schizencephaly
Polymicrogyria and Schizencephaly
Predominantly Antibody Deficiency
Predominantly Antibody Deficiency
Prepair 1000+
Prepair 1000+
Prepair 500+
Prepair 500+
Primary Ovarian Insufficiency_Premature Ovarian Failure
Primary Ovarian Insufficiency_Premature Ovarian Failure
Progressive Myoclonic Epilepsy
Progressive Myoclonic Epilepsy
Progressive Neurological Conditions
Proteinuria
Proteinuria
Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy
Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy
Pulmonary Arterial Hypertension
Pulmonary Arterial Hypertension
Pulmonary Fibrosis_Interstitial Lung Disease
Pulmonary Fibrosis_Interstitial Lung Disease
Radial Ray Abnormalities
Radial Ray Abnormalities
Rasopathy
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Red cell disorders
Red cell disorders
Regression
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Renal cancer
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Renal Cystic Disease_SuperPanel
Renal Glomerular Disease_SuperPanel
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Renal Macrocystic Disease
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Renal Tubulointerstitial Disease
Renal Tubulopathies and related disorders
Renal Tubulopathies and related disorders
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Retinal Disorders Superpanel
Retinitis pigmentosa_Autosomal Recessive/X-linked
Retinitis pigmentosa_Autosomal Recessive/X-linked
Retinitis pigmentosa_Autosomal Dominant
Retinitis pigmentosa_Autosomal Dominant
Retinitis Pigmentosa Superpanel
Rhabdomyolysis and Metabolic Myopathy
Rhabdomyolysis and Metabolic Myopathy
Sarcoma
Sarcoma
Schwannomatosis
Schwannomatosis
Severe Combined Immunodeficiency (absent T present B cells)
Severe Combined Immunodeficiency (absent T present B cells)
Severe Combined Immunodeficiency (absent T absent B cells)
Severe Combined Immunodeficiency (absent T absent B cells)
Severe early-onset obesity
Severe early-onset obesity
Short Long Bones with Advanced Carpal Bone Age
Short Long Bones with Advanced Carpal Bone Age
Short QT syndrome
Short QT syndrome
Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy
Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy
Sick sinus syndrome
Sick sinus syndrome
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Skeletal Dysplasia_Fetal
Skeletal Dysplasia_Fetal
Skeletal Muscle Channelopathies
Skeletal Muscle Channelopathies
Speech apraxia
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Spondylocostal Dysostosis
Spondylocostal Dysostosis
Stickler Syndrome
Stickler Syndrome
Stroke
Stroke
Susceptibility to Fungal Infections
Susceptibility to Fungal Infections
Susceptibility to Viral Infections
Susceptibility to Viral Infections
Syndromic Retinopathy
Syndromic Retinopathy
TCGA_PANCAN_2018
TCGA_PANCAN_2018
Transplant Co-Morbidity Superpanel
Transplant Co-Morbidity Superpanel
Tremors_Superpanel
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
Tubulinopathies
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Vascular Malformations SuperPanel
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Vitamin metabolism disorders
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Vitreoretinopathy
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Wilms Tumour Predisposition
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2.0
Gene or Genomic Entity Name
SYNE1
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05 Feb 2026
Limb-Girdle Muscular Dystrophy and Distal Myopathy v2.0
SYNE1
Gene migrated from ENSG00000131018 to ENSG00000131018 (gene set migration)