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Achromatopsia
Additional findings_Adult
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Adrenal insufficiency
Adult Cardiac SuperPanel
Alagille syndrome
Alternating Hemiplegia and Hemiplegic Migraine
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Deafness_IsolatedAndComplex
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Hereditary angioedema
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IBMDx study
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Incidentalome
Incidentalome_PREGEN_DRAFT
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Kabuki syndrome
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Kidneyome_SuperPanel
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Limb and Digital Malformations SuperPanel
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Lipodystrophy_Lipoatrophy
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Liverome Superpanel
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Mackenzie's Mission_Reproductive Carrier Screening
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Myopathy Superpanel
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Pierre Robin Sequence
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Polycystic liver disease
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Prepair 1000+
Prepair 500+
Primary nodular adrenocortical disease
Primary Ovarian Insufficiency_Premature Ovarian Failure
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Progressive Neurological Conditions
Prostate Cancer
Proteinuria
Pseudohypoparathyroidism and Albright Hereditary Osteodystrophy
Pulmonary Arterial Hypertension
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Renal Cystic Disease_SuperPanel
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Retinal Disorders Superpanel
Retinitis pigmentosa
Rhabdomyolysis and Metabolic Myopathy
Sarcoma non-soft tissue
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Schwannoma
Severe Combined Immunodeficiency
Severe early-onset obesity
Short QT syndrome
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Skeletal dysplasia
Skeletal Dysplasia_Fetal
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Speech apraxia
Spontaneous coronary artery dissection
Stickler Syndrome
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Susceptibility to Viral Infections
Syndromic Retinopathy
Thyroid Cancer
Transplant Co-Morbidity
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly
Tubulinopathies
Usher Syndrome
Vascular Malformations_Germline
Vascular Malformations_Somatic
Vascular Malformations SuperPanel
Vitamin metabolism disorders
Vitreoretinopathy
Wilms Tumour
Version
Panel Version
2.268
1.5025
Gene or Genomic Entity Name
POPDC1
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25 Jun 2026
Mendeliome v2.106
POPDC1
Zornitza Stark Tag new gene name tag was added to gene: POPDC1.
07 Jun 2026
Mendeliome v2.0
POPDC1
Gene symbol changed from BVES to POPDC1 during gene set migration (ENSG00000112276 -> ENSG00000112276)