constrain to be
IN
NOT IN saved Gene list
PL_BHF_UCL_cardiovascGenes
PL_DiabesityGWAS_pval-4
PL_DiabetesGenes
PL_GenomicsEngland_GenePanel:Adult_solid_tumours_for_rare_disease
PL_GenomicsEngland_GenePanel:Amelogenesis_imperfecta
PL_GenomicsEngland_GenePanel:Amyotrophic_lateral_sclerosis/motor_neuron_disease
PL_GenomicsEngland_GenePanel:Anophthalmia_or_microphthalmia
PL_GenomicsEngland_GenePanel:Arrhythmogenic_cardiomyopathy
PL_GenomicsEngland_GenePanel:Arthrogryposis
PL_GenomicsEngland_GenePanel:Atypical_haemolytic_uraemic_syndrome
PL_GenomicsEngland_GenePanel:Auditory_Neuropathy_Spectrum_Disorder
PL_GenomicsEngland_GenePanel:Autosomal_recessive_congenital_ichthyosis
PL_GenomicsEngland_GenePanel:Beckwith-Wiedemann_syndrome_(BWS)_and_other_congenital_overgrowth_disorders
PL_GenomicsEngland_GenePanel:Brain_channelopathy
PL_GenomicsEngland_GenePanel:Brugada_syndrome
PL_GenomicsEngland_GenePanel:CAKUT
PL_GenomicsEngland_GenePanel:Cataracts
PL_GenomicsEngland_GenePanel:Catecholaminergic_polymorphic_VT
PL_GenomicsEngland_GenePanel:Cerebellar_hypoplasia
PL_GenomicsEngland_GenePanel:Cerebral_folate_deficiency
PL_GenomicsEngland_GenePanel:Cerebral_vascular_malformations
PL_GenomicsEngland_GenePanel:Choanal_atresia
PL_GenomicsEngland_GenePanel:Chondrodysplasia_punctata
PL_GenomicsEngland_GenePanel:Classical_tuberous_sclerosis
PL_GenomicsEngland_GenePanel:Clefting
PL_GenomicsEngland_GenePanel:Congenital_adrenal_hypoplasia
PL_GenomicsEngland_GenePanel:Congenital_disorders_of_glycosylation
PL_GenomicsEngland_GenePanel:Congenital_hyperinsulinism
PL_GenomicsEngland_GenePanel:Congenital_hypothyroidism
PL_GenomicsEngland_GenePanel:Congenital_muscular_dystrophy
PL_GenomicsEngland_GenePanel:Congenital_myaesthenic_syndrome
PL_GenomicsEngland_GenePanel:Congenital_myopathy
PL_GenomicsEngland_GenePanel:Corneal_abnormalities
PL_GenomicsEngland_GenePanel:Craniosynostosis
PL_GenomicsEngland_GenePanel:Currarino_triad
PL_GenomicsEngland_GenePanel:Cystic_kidney_disease
PL_GenomicsEngland_GenePanel:Cytopenias_and_congenital_anaemias
PL_GenomicsEngland_GenePanel:Deafness_and_congenital_structural_abnormalities
PL_GenomicsEngland_GenePanel:Diabetes_-_neonatal_onset
PL_GenomicsEngland_GenePanel:Diabetes_with_additional_phenotypes_suggestive_of_a_monogenic_aetiology
PL_GenomicsEngland_GenePanel:Dilated_Cardiomyopathy_and_conduction_defects
PL_GenomicsEngland_GenePanel:Disorders_of_sex_development
PL_GenomicsEngland_GenePanel:Distal_myopathies
PL_GenomicsEngland_GenePanel:Ductal_plate_malformation
PL_GenomicsEngland_GenePanel:Early_onset_dementia_(encompassing_fronto-temporal_dementia_and_prion_disease)
PL_GenomicsEngland_GenePanel:Early_onset_dystonia
PL_GenomicsEngland_GenePanel:Ectodermal_dysplasia_without_a_known_gene_mutation
PL_GenomicsEngland_GenePanel:Ehlers_Danlos_syndromes
PL_GenomicsEngland_GenePanel:Epidermolysis_bullosa
PL_GenomicsEngland_GenePanel:Erythropoietic_protoporphyria,_mild_variant
PL_GenomicsEngland_GenePanel:Extreme_early-onset_hypertension
PL_GenomicsEngland_GenePanel:Familial_Hirschsprung_Disease
PL_GenomicsEngland_GenePanel:Familial_Meniere_Disease
PL_GenomicsEngland_GenePanel:Familial_Neural_Tube_Defects
PL_GenomicsEngland_GenePanel:Familial_Tumours_Syndromes_of_the_central_&_peripheral_Nervous_system
PL_GenomicsEngland_GenePanel:Familial_breast_cancer
PL_GenomicsEngland_GenePanel:Familial_cerebral_small_vessel_disease
PL_GenomicsEngland_GenePanel:Familial_cicatricial_alopecia
PL_GenomicsEngland_GenePanel:Familial_diabetes
PL_GenomicsEngland_GenePanel:Familial_disseminated_superficial_actinic_porokeratosis
PL_GenomicsEngland_GenePanel:Familial_dysautonomia
PL_GenomicsEngland_GenePanel:Familial_hidradenitis_suppurativa
PL_GenomicsEngland_GenePanel:Familial_hypercholesterolaemia
PL_GenomicsEngland_GenePanel:Familial_hyperparathyroidism
PL_GenomicsEngland_GenePanel:Familial_hypoparathyroidism
PL_GenomicsEngland_GenePanel:Familial_non_syndromic_congenital_heart_disease
PL_GenomicsEngland_GenePanel:Familial_prostate_cancer
PL_GenomicsEngland_GenePanel:Familial_pulmonary_fibrosis
PL_GenomicsEngland_GenePanel:Familial_rhabdomyosarcoma
PL_GenomicsEngland_GenePanel:Fetal_hydrops
PL_GenomicsEngland_GenePanel:GI_tract_tumours
PL_GenomicsEngland_GenePanel:Gastrointestinal_epithelial_barrier_disorders
PL_GenomicsEngland_GenePanel:Gastrointestinal_neuromuscular_disorders
PL_GenomicsEngland_GenePanel:Generalised_pustular_psoriasis
PL_GenomicsEngland_GenePanel:Genetic_epilepsy_syndromes
PL_GenomicsEngland_GenePanel:Genodermatoses_with_malignancies
PL_GenomicsEngland_GenePanel:Glaucoma_(developmental)
PL_GenomicsEngland_GenePanel:Haematological_malignancies_for_rare_disease
PL_GenomicsEngland_GenePanel:Haematuria
PL_GenomicsEngland_GenePanel:Hearing_loss
PL_GenomicsEngland_GenePanel:Hereditary_Erythrocytosis
PL_GenomicsEngland_GenePanel:Hereditary_ataxia
PL_GenomicsEngland_GenePanel:Hereditary_haemorrhagic_telangiectasia
PL_GenomicsEngland_GenePanel:Hereditary_neuropathy
PL_GenomicsEngland_GenePanel:Hereditary_spastic_paraplegia
PL_GenomicsEngland_GenePanel:Holoprosencephaly
PL_GenomicsEngland_GenePanel:Hydroa_vacciniforme
PL_GenomicsEngland_GenePanel:Hydrocephalus
PL_GenomicsEngland_GenePanel:Hyperammonaemia
PL_GenomicsEngland_GenePanel:Hyperthyroidism
PL_GenomicsEngland_GenePanel:Hypertrophic_cardiomyopathy_-_teen_and_adult
PL_GenomicsEngland_GenePanel:Hypogonadotropic_hypogonadism
PL_GenomicsEngland_GenePanel:IUGR_and_IGF_abnormalities
PL_GenomicsEngland_GenePanel:Idiopathic_ventricular_fibrillation
PL_GenomicsEngland_GenePanel:Infantile_enterocolitis_&_monogenic_inflammatory_bowel_disease
PL_GenomicsEngland_GenePanel:Infantile_nystagmus
PL_GenomicsEngland_GenePanel:Inherited_bleeding_disorders
PL_GenomicsEngland_GenePanel:Inherited_non-medullary_thyroid_cancer
PL_GenomicsEngland_GenePanel:Inherited_ovarian_cancer_(without_breast_cancer)
PL_GenomicsEngland_GenePanel:Inherited_phaeochromocytoma_and_paraganglioma
PL_GenomicsEngland_GenePanel:Inherited_white_matter_disorders
PL_GenomicsEngland_GenePanel:Insulin_resistance_(including_lipodystrophy)
PL_GenomicsEngland_GenePanel:Intellectual_disability
PL_GenomicsEngland_GenePanel:Intracerebral_calcification_disorders
PL_GenomicsEngland_GenePanel:Juvenile_dermatomyositis
PL_GenomicsEngland_GenePanel:Kabuki_syndrome
PL_GenomicsEngland_GenePanel:Ketotic_hypoglycaemia
PL_GenomicsEngland_GenePanel:Kleine-Levin_syndrome
PL_GenomicsEngland_GenePanel:Left_Ventricular_Noncompaction_Cardiomyopathy
PL_GenomicsEngland_GenePanel:Limb_disorders
PL_GenomicsEngland_GenePanel:Limb_girdle_muscular_dystrophy
PL_GenomicsEngland_GenePanel:Long_QT_syndrome
PL_GenomicsEngland_GenePanel:Malformations_of_cortical_development
PL_GenomicsEngland_GenePanel:Membranoproliferative_glomerulonephritis
PL_GenomicsEngland_GenePanel:Mitochondrial_disorders
PL_GenomicsEngland_GenePanel:Monogenic_nephrogenic_diabetes_insipidus
PL_GenomicsEngland_GenePanel:Mucopolysaccharideosis,_Gaucher,_Fabry
PL_GenomicsEngland_GenePanel:Multi-organ_autoimmune_diabetes
PL_GenomicsEngland_GenePanel:Multiple_Epiphyseal_Dysplasia
PL_GenomicsEngland_GenePanel:Multiple_endocrine_tumours
PL_GenomicsEngland_GenePanel:Multiple_lipomas
PL_GenomicsEngland_GenePanel:Neonatal_cholestasis
PL_GenomicsEngland_GenePanel:Nephrocalcinosis_or_nephrolithiasis
PL_GenomicsEngland_GenePanel:Neurofibromatosis_Type_1
PL_GenomicsEngland_GenePanel:Neurotransmitter_disorders
PL_GenomicsEngland_GenePanel:Non-CF_bronchiectasis
PL_GenomicsEngland_GenePanel:Non-syndromic_familial_congenital_anorectal_malformations
PL_GenomicsEngland_GenePanel:Non-syndromic_hypotrichosis
PL_GenomicsEngland_GenePanel:Ocular_and_oculo-cutaneous_albinism
PL_GenomicsEngland_GenePanel:Ocular_coloboma
PL_GenomicsEngland_GenePanel:Optic_neuropathy
PL_GenomicsEngland_GenePanel:Osteogenesis_imperfecta
PL_GenomicsEngland_GenePanel:PHACE(S)_syndrome
PL_GenomicsEngland_GenePanel:Paediatric_motor_neuronopathies
PL_GenomicsEngland_GenePanel:Pain_syndromes
PL_GenomicsEngland_GenePanel:Palmoplantar_keratoderma_and_erythrokeratodermas
PL_GenomicsEngland_GenePanel:Pancreatitis
PL_GenomicsEngland_GenePanel:Parathyroid_Cancer
PL_GenomicsEngland_GenePanel:Parkinson_Disease_and_Complex_Parkinsonism
PL_GenomicsEngland_GenePanel:Peeling_skin_syndrome
PL_GenomicsEngland_GenePanel:Periodic_fever_syndromes
PL_GenomicsEngland_GenePanel:Peroxisomal_disorders
PL_GenomicsEngland_GenePanel:Pityriasis_rubra_pilaris
PL_GenomicsEngland_GenePanel:Pneumothorax_-_familial
PL_GenomicsEngland_GenePanel:Primary_ciliary_disorders
PL_GenomicsEngland_GenePanel:Primary_immunodeficiency
PL_GenomicsEngland_GenePanel:Primary_lymphoedema
PL_GenomicsEngland_GenePanel:Primary_ovarian_insufficiency
PL_GenomicsEngland_GenePanel:Proteinuric_renal_disease
PL_GenomicsEngland_GenePanel:Pulmonary_arterial_hypertension
PL_GenomicsEngland_GenePanel:RASopathies
PL_GenomicsEngland_GenePanel:Radial_dysplasia
PL_GenomicsEngland_GenePanel:Rare_multisystem_ciliopathy_disorders
PL_GenomicsEngland_GenePanel:Renal_tubulopathies
PL_GenomicsEngland_GenePanel:Retinal_disorders
PL_GenomicsEngland_GenePanel:Rhabdomyolysis_and_metabolic_muscle_disorders
PL_GenomicsEngland_GenePanel:Segmental_overgrowth_disorders
PL_GenomicsEngland_GenePanel:Severe_early-onset_obesity
PL_GenomicsEngland_GenePanel:Severe_familial_anorexia
PL_GenomicsEngland_GenePanel:Severe_hypertriglyceridaemia
PL_GenomicsEngland_GenePanel:Severe_microcephaly
PL_GenomicsEngland_GenePanel:Severe_multi-system_atopic_disease_with_high_IgE
PL_GenomicsEngland_GenePanel:Short_QT_syndrome
PL_GenomicsEngland_GenePanel:Silver_Russell_syndrome
PL_GenomicsEngland_GenePanel:Skeletal_Muscle_Channelopathies
PL_GenomicsEngland_GenePanel:Skeletal_dysplasia
PL_GenomicsEngland_GenePanel:Stickler_syndrome
PL_GenomicsEngland_GenePanel:Structural_basal_ganglia_disorders
PL_GenomicsEngland_GenePanel:Sudden_death_in_young_people
PL_GenomicsEngland_GenePanel:Thoracic_aortic_aneurysm_or_dissection
PL_GenomicsEngland_GenePanel:Thoracic_dystrophies
PL_GenomicsEngland_GenePanel:Tumour_predisposition_-_childhood_onset
PL_GenomicsEngland_GenePanel:Ultra-rare_undescribed_monogenic_disorders
PL_GenomicsEngland_GenePanel:Undiagnosed_metabolic_disorders
PL_GenomicsEngland_GenePanel:Unexplained_kidney_failure_in_young_people
PL_GenomicsEngland_GenePanel:VACTERL-like_phenotypes
PL_GenomicsEngland_GenePanel:Vici_Syndrome_and_other_autophagy_disorders
PL_GenomicsEngland_GenePanel:Xeroderma_pigmentosum,_Trichothiodystrophy_or_Cockayne_syndrome
PL_IntermineUseCase_geneList
PL_Pax6_Targets
PL_PraderWilliRegion_Genes
PL_Protein coding cancer genes containing probable driver mutations
PL_monogenGlucTolerance_ORahilly09
PL_obesityLociReview_Day2011
PL_obesityMonogen_ORahilly09