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GeneThis summary box displays a gene, condition, or laboratory matching your search query. | PAX2-paired box 2 |
| Also know as: FSGS7, PAPRS, PAX-2; GeneID:5076; Location:10q24.31; | |
| Associated conditions: Anophthalmia-microphthalmia syndrome; Focal segmental glomerulosclerosis 7; Renal coloboma syndrome |
Labs matching your search
32 labs with tests matching your search, 4 labs matching in other ways
Results:
108 genetic tests from 32 labs with tests matching your search, 4 labs matching in other ways
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods | |
|---|---|---|---|---|
| 470 | 449 |
| ||
PAX2 Gene Focal segmental glomerulosclerosis type 7 NGS Genetic DNA Test | 1 | 1 |
| |
| 1 | 1 |
| ||
| 1 | 299 |
| ||
| 25 | 56 |
| ||
| 16 | 44 |
| ||
| 2 | 1 |
| ||
Multigene panel for hearing loss based on whole-exome sequencing | 1 | 222 |
| |
| 693 | 388 |
| ||
| 27 | 58 |
| ||
| 1654 | 1199 |
| ||
Invitae Nephrotic Syndrome and Focal Segmental Glomerulosclerosis (FSGS) Panel | 81 | 57 |
| |
Invitae Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Panel | 67 | 41 |
| |
| 96 | 44 |
| ||
| 27 | 32 |
| ||
Nephrotic syndrome and related disorders Comprehensive panel | 27 | 32 |
| |
Nephrotic syndrome and related disorders Deletion / Duplication panel | 27 | 32 |
| |
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
|
108 tests from 32 labs
Page 1 of 6❯RenaDx™: Comprehensive Renal Disease Genetics Panel by Precision Medicine Care (PMC®)
470 conditions, 449 genes
470 conditions, 449 genes
PAX2 Gene Papillorenal syndrome NGS Genetic DNA Test by DNA Labs India
1 condition, 1 gene
1 condition, 1 gene
Comprehensive Nephrology Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 299 genes
1 condition, 299 genes
FSGS/Nephrotic Syndrome Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
25 conditions, 56 genes
25 conditions, 56 genes
Cystic Kidney Disease Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
16 conditions, 44 genes
16 conditions, 44 genes
PAX2 sequencing by University of Minnesota Physicians Outreach Laboratory, University of Minnesota
2 conditions, 1 gene
2 conditions, 1 gene
Multigene panel for hearing loss based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 222 genes
1 condition, 222 genes
Invitae Expanded Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
693 conditions, 388 genes
693 conditions, 388 genes
GenepoweRx_Nephro_Care by GenepoweRx, Uppaluri K&H Personalized Medicine Clinic
27 conditions, 58 genes
27 conditions, 58 genes
MVL Vision Panel by Molecular Vision Laboratory
1654 conditions, 1199 genes
1654 conditions, 1199 genes
Invitae Nephrotic Syndrome and Focal Segmental Glomerulosclerosis (FSGS) Panel by Labcorp Genetics (formerly Invitae), LabCorp
81 conditions, 57 genes
81 conditions, 57 genes
Invitae Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Panel by Labcorp Genetics (formerly Invitae), LabCorp
67 conditions, 41 genes
67 conditions, 41 genes
Invitae Cystic Kidney Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
96 conditions, 44 genes
96 conditions, 44 genes
Nephrotic syndrome and related disorders NGS panel by HNL Genomics Connective Tissue Gene Tests
27 conditions, 32 genes
27 conditions, 32 genes
Nephrotic syndrome and related disorders Comprehensive panel by HNL Genomics Connective Tissue Gene Tests
27 conditions, 32 genes
27 conditions, 32 genes
Nephrotic syndrome and related disorders Deletion / Duplication panel by HNL Genomics Connective Tissue Gene Tests
27 conditions, 32 genes
27 conditions, 32 genes
Glomerulosclerosis, focal segmental, 7, 616002, Autosomal dominant; FSGS7 (Familial idiopathic steroid-resistant nephrotic syndrome) (PAX2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Papillorenal syndrome, 120330, Autosomal dominant; PAPRS (Renal coloboma syndrome) (PAX2 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Papillorenal syndrome, 120330, Autosomal dominant; PAPRS (Renal coloboma syndrome) (PAX2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
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