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Alagille syndrome
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Alternating Hemiplegia and Hemiplegic Migraine
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Amelogenesis imperfecta
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Angelman Rett like syndromes
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Brugada syndrome
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Cardiomyopathy_Adult_SuperPanel
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Catecholaminergic Polymorphic Ventricular Tachycardia
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Cerebellar and Pontocerebellar Hypoplasia
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Cerebral amyloid angiopathy
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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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Metal Metabolism Disorders
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Mirror movements
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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
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Peroxisomal Disorders
Phagocyte Defects
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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
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Polydactyly
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
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Pulmonary Fibrosis_Interstitial Lung Disease
Radial Ray Abnormalities
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Red cell disorders
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Retinal Disorders Superpanel
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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
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Skeletal Muscle Channelopathies
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Speech apraxia
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Stickler Syndrome
Stickler Syndrome
Stroke
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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
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2.0
Gene or Genomic Entity Name
TIA1
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05 Feb 2026
Limb-Girdle Muscular Dystrophy and Distal Myopathy v2.0
TIA1
Gene migrated from ENSG00000116001 to ENSG00000116001 (gene set migration)