CDC73:Ensemblv90

cell division cycle 73
OMIM: 607393, ClinGen, DECIPHER

17 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 17 panels
Green CDC73 in Hypercalcaemia Level 2: Endocrine disorders Version 1.2	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000
Green CDC73 in Mendeliome Version 1.3802	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000
Red CDC73 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.132	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Parathyroid carcinoma, MIM# 608266
Green CDC73 in Calcium and Phosphate disorders Level 2: Renal and urinary tract disorders; Endocrine disorders Version 1.29	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green KidGen_CalcPhos v38.1.0 Victorian Clinical Genetics Services Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000
Green CDC73 in Additional findings_Adult Level 2: Screening Version 1.130	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000
Amber CDC73 in Wilms Tumour Predisposition Level 2: Cancer predisposition Version 0.40	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Hyperparathyroidism-jaw tumor syndrome, MIM# 145001
Red CDC73 in CGC_86 Version 0.3	0 reviews	Other	Sources CGC_86 Phenotypes Hyperparathyroidism 2
Red CDC73 in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes Hyperparathyroidism 2
Red CDC73 in TCGA_PANCAN_2018 Version 0.3	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Hyperparathyroidism 2
Green CDC73 in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.22 Component of the following Super Panels: Kidneyome_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green KidGen_CalcPhos v38.1.0 Expert Review Green Expert Review Green Expert Review Green KidGen_CalcPhos v38.1.0 Victorian Clinical Genetics Services Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000
Green CDC73 in Hypercalcaemia Level 2: Endocrine disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000
Red CDC73 in Cancer Predisposition_Paediatric Level 2: Cancer Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Red Phenotypes Parathyroid carcinoma, MIM# 608266
Green CDC73 in Calcium and Phosphate disorders Level 2: Renal and urinary tract disorders; Endocrine disorders Version 2.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services KidGen_CalcPhos v38.1.0 Expert Review Green Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000
Green CDC73 in Additional findings_Adult Level 2: Screening Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000
Amber CDC73 in Wilms Tumour Predisposition Level 2: Cancer predisposition Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Amber Phenotypes Hyperparathyroidism-jaw tumor syndrome, MIM# 145001
Red CDC73 in TCGA_PANCAN_2018 Version 1.0	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Hyperparathyroidism 2
Green CDC73 in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 2.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services KidGen_CalcPhos v38.1.0 Expert Review Green Expert Review Green Expert Review Green KidGen_CalcPhos v38.1.0 Expert Review Green Phenotypes Hyperparathyroidism-jaw tumour syndrome, MIM# 145001 Hyperparathyroidism, familial primary, MIM# 145000