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Gene

MAMLD1-mastermind like domain containing 1
Also know as: CG1, CXorf6, F18, HYSP2; GeneID:10046; Location:Xq28;
Associated condition: Hypospadias 2, X-linked
Results:
40 genetic tests from 19 labs with tests matching your search, 3 labs matching in other ways
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Tests names and labsConditionsGenes, analytes, and microbesMethods

MAMLD1 Gene Hypospadias type 2, X-linked NGS Genetic DNA Test

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

High-Resolution Rapid Microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

MayoComplete Sarcoma Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
31441
  • R RNA analysis
  • E Sequence analysis of select exons

Neuro-Onc Panel, Fusions Only

Mayo Clinic Laboratories, Mayo Clinic
United States
181
  • E Sequence analysis of select exons

MayoComplete Targeted RNAseq Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
11441
  • R RNA analysis

Neuro-Onc Expanded Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
11441
  • R RNA 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 Disorders of Sex Development Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
8853
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypospadias 2, X-linked, 300758, X-linked recessive; HYSP2 (Familial hypospadias) (MAMLD1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Hypospadias 2, X-linked, 300758, X-linked recessive; HYSP2 (Familial hypospadias) (MAMLD1 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 Sex development disorders

Quantitative Genomic Medicine Laboratories, SL
Spain
4548
  • C Sequence analysis of the entire coding region

X-chromosome High Resolution microarray analysis

Pittsburgh Cytogenetics Laboratory, University of Pittsburgh Medical Center
United States
240171
  • D Deletion/duplication analysis

Disorders of Sex Development Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center, Oregon Health & Science University
United States
3108
  • C Sequence analysis of the entire coding region

Differences in sexual development panel

CGC Genetics, Unilabs
Portugal
1100
  • C Sequence analysis of the entire coding region

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
1250
  • E Sequence analysis of select exons

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
1416
  • E Sequence analysis of select exons

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
1526
  • E Sequence analysis of select exons

Exome Panel Sequencing and CNVs

Laboratorio de Genetica Clinica SL
Spain
1105
  • E Sequence analysis of select exons

Sanger sequencing of MAMLD1

Laboratorio de Genetica Clinica SL
Spain
11
  • E Sequence analysis of select exons
40 tests from 19 labs
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Page 1 of 2
MayoComplete Sarcoma Panel by Mayo Clinic Laboratories, Mayo Clinic
3 conditions, 1441 genes
Neuro-Onc Panel, Fusions Only by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 81 genes
MayoComplete Targeted RNAseq Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 1441 genes
Neuro-Onc Expanded Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 1441 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
Invitae Disorders of Sex Development Panel by Labcorp Genetics (formerly Invitae), LabCorp
88 conditions, 53 genes
qGenEx Sex development disorders by Quantitative Genomic Medicine Laboratories, SL
45 conditions, 48 genes
X-chromosome High Resolution microarray analysis by Pittsburgh Cytogenetics Laboratory, University of Pittsburgh Medical Center
240 conditions, 171 genes
Disorders of Sex Development Panel by Knight Diagnostic Laboratories - Molecular Diagnostic Center, Oregon Health & Science University
3 conditions, 108 genes
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 250 genes
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 416 genes
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 526 genes
Exome Panel Sequencing and CNVs by Laboratorio de Genetica Clinica SL
1 condition, 105 genes
Sanger sequencing of MAMLD1 by Laboratorio de Genetica Clinica SL
1 condition, 1 gene

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.