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Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic
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Mackenzie's Mission_Reproductive Carrier Screening
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Mandibulofacial Acrofacial dysostosis
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Maturity-onset Diabetes of the Young
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Metal Metabolism Disorders
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Microcephalic Primordial Dwarfism and Slender bone dysplasias
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Miscellaneous Metabolic Disorders
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Monogenic Diabetes
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Motor Neurone Disease
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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
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Neurodegeneration with brain iron accumulation
Neurodegenerative disease - adult onset
Neuromuscular Superpanel
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Neurotransmitter Defects
Nucleotide metabolism disorders
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Ocular and Oculocutaneous Albinism
Ocular and Oculocutaneous Albinism
Oligodontia
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Optic Atrophy
Optic Atrophy
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Osteogenesis Imperfecta and Osteoporosis
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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
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Pituitary hormone deficiency
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Polycystic liver disease
Polycystic liver disease
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Polymicrogyria and Schizencephaly
Polymicrogyria and Schizencephaly
Predominantly Antibody Deficiency
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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
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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
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Renal cancer
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Renal Tubulointerstitial Disease
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Retinal Disorders Superpanel
Retinitis pigmentosa_Autosomal Recessive/X-linked
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Retinitis Pigmentosa Superpanel
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Rhabdomyolysis and Metabolic Myopathy
Sarcoma
Sarcoma
Schwannomatosis
Schwannomatosis
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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 Muscle Channelopathies
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Speech apraxia
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Spondylocostal Dysostosis
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Stickler Syndrome
Stickler Syndrome
Stroke
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Susceptibility to Fungal Infections
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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
BANF1
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05 Feb 2026
Hereditary Neuropathy_CMT - isolated v2.0
BANF1
Gene migrated from ENSG00000175334 to ENSG00000175334 (gene set migration)