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Gene

CISD2-CDGSH iron sulfur domain 2
Also know as: ERIS, Miner1, NAF-1, WFS2, ZCD2; GeneID:493856; Location:4q24;
Associated condition: Wolfram syndrome 2

Labs matching your search


32 labs with tests matching your search, 1 lab matching in other ways
Results:
85 genetic tests from 32 labs with tests matching your search, 1 lab matching in other ways
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Tests names and labsConditionsGenes, analytes, and microbesMethods

RenaDx™: Comprehensive Renal Disease Genetics Panel

Precision Medicine Care (PMC®)
United States
470449
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Diabetes Panel

Genetic Services Laboratory, University of Chicago
United States
343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Wolfram syndrome panel

Genetic Services Laboratory, University of Chicago
United States
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CISD2 Gene Wolfram syndrome type 2 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

OtoSCOPE v9

Molecular Otolaryngology and Renal Research Laboratories, University of Iowa Hospital and Clinics
United States
284218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Multigene panel for hearing loss based on whole-exome sequencing

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
1222
  • S Mutation scanning of the entire coding region

Genomic Unity® Hearing Loss Disorders Analysis

Variantyx, Inc.
United States
1318
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Invitae Expanded Renal Disease Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
693388
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Genomic Unity® Nuclear Encoded Mitochondrial Gene Analysis

Variantyx, Inc.
United States
1335
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

AudioloGene Hearing Loss Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
1200
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
16541199
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoNeuro Panel

CENTOGENE GmbH and LLC - Guiding Precision Medicine
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Deafness Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
404219
  • D Deletion/duplication analysis

Wolfram syndrome 2, 604928, Autosomal recessive; WFS2 (Wolfram syndrome) (CISD2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

qGenEx Intellectual disability

Quantitative Genomic Medicine Laboratories, SL
Spain
31969
  • S Mutation scanning of the entire coding region
  • C Sequence analysis of the entire coding region

Invitae Inherited Retinal Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
485293
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Optic Atrophy

Amplexa Genetics, Amplexa Genetics A/S
Denmark
115
  • S Mutation scanning of the entire coding region

Comprehensive Neonatal Diabetes Mutation Analysis

Genetic Services Laboratory, University of Chicago
United States
541
  • D Deletion/duplication analysis
  • M Methylation analysis
  • C Sequence analysis of the entire coding region

Monogenic Diabetes Panel

Genetic Services Laboratory, University of Chicago
United States
1473
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
161
  • E Sequence analysis of select exons
85 tests from 32 labs
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Page 1 of 5
Neonatal Diabetes Panel by Genetic Services Laboratory, University of Chicago
3 conditions, 43 genes
Wolfram syndrome panel by Genetic Services Laboratory, University of Chicago
2 conditions, 2 genes
OtoSCOPE v9 by Molecular Otolaryngology and Renal Research Laboratories, University of Iowa Hospital and Clinics
284 conditions, 218 genes
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
Invitae Expanded Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
693 conditions, 388 genes
AudioloGene Hearing Loss Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 200 genes
MVL Vision Panel by Molecular Vision Laboratory
1654 conditions, 1199 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
Invitae Comprehensive Deafness Panel by Labcorp Genetics (formerly Invitae), LabCorp
404 conditions, 219 genes
qGenEx Intellectual disability by Quantitative Genomic Medicine Laboratories, SL
3 conditions, 1969 genes
Invitae Inherited Retinal Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
485 conditions, 293 genes
Optic Atrophy by Amplexa Genetics, Amplexa Genetics A/S
1 condition, 15 genes
Comprehensive Neonatal Diabetes Mutation Analysis by Genetic Services Laboratory, University of Chicago
5 conditions, 41 genes
Monogenic Diabetes Panel by Genetic Services Laboratory, University of Chicago
14 conditions, 73 genes
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 61 genes

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.