MNX1 gene related symptoms and diseases
All the information presented here about the MNX1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to MNX1 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Hypospadias | Very Common - Between 80% and 100% cases |
| Vesicoureteral reflux | Very Common - Between 80% and 100% cases |
| Hypoplasia of penis | Very Common - Between 80% and 100% cases |
| Abnormal intestine morphology | Very Common - Between 80% and 100% cases |
| Bifid scrotum | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with MNX1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Male pseudohermaphroditism
- Arteriovenous malformation
- Lower limb asymmetry
- Sacrococcygeal teratoma
- Aplasia/Hypoplasia of the sacrum
Rare diseases associated to MNX1 gene
Here you will find a list of rare diseases related to the MNX1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CURRARINO SYNDROME
Alternate names
CURRARINO SYNDROME Is also known as currarino triad
Description
Currarino syndrome (CS) is a rare congenital disease characterized by the triad of anorectal malformations (ARMs) (usually anal stenosis), presacral mass (commonly anterior sacral meningocele (ASM) or teratoma) and sacral anomalies (i.e. total or partial agenesis of the sacrum and coccyx or deformity of the sacral vertebrae).
Most common symptoms of CURRARINO SYNDROME
- Hypospadias
- Vesicoureteral reflux
- Hypoplasia of penis
- Abnormal intestine morphology
- Bifid scrotum
More info about CURRARINO SYNDROME
SOURCES: ORPHANET
Search interest in MNX1
Potential gene panels for MNX1 gene
Neonatal Diabetes Mellitus and Maturity-Onset Diabetes of the Young Deletion/Duplication Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Neonatal Diabetes Mellitus and Maturity-Onset Diabetes of the Young Deletion/Duplication Panel that also includes the following genes: BLK SLC2A2 STAT3 KLF11 WFS1 ZBTB20 NEUROG3 LRBA CDKN1C CEL
More info about this panel United States.
Neonatal Diabetes Mellitus and Maturity-Onset Diabetes of the Young Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Neonatal Diabetes Mellitus and Maturity-Onset Diabetes of the Young Panel that also includes the following genes: BLK SLC2A2 STAT3 KLF11 WFS1 ZBTB20 NEUROG3 LRBA CDKN1C CEL
More info about this panel United States.
Comprehensive Neonatal Diabetes Mutation Analysis Panel
United States.
By Genetic Services Laboratory University of Chicago Comprehensive Neonatal Diabetes Mutation Analysis that also includes the following genes: ZFP57 EIF2AK3 GATA4 GATA6 GCK MNX1 HYMAI ABCC8 INS FOXP3
More info about this panel United States.
Neonatal Diabetes Mellitus Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Neonatal Diabetes Mellitus Sequencing Panel that also includes the following genes: ZFP57 EIF2AK3 GATA4 GATA6 GCK MNX1 ABCC8 INS FOXP3 PDX1
More info about this panel United States.
MNX1 sequencing Panel
United States.
By Genetic Services Laboratory University of Chicago
This panel specifically test the MNX1 gene.
More info about this panel United States.
MNX1 deletion/duplication analysis Panel
United States.
By Genetic Services Laboratory University of Chicago
This panel specifically test the MNX1 gene.
More info about this panel United States.
HLXB9. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the MNX1 gene.
More info about this panel Spain.
Currarino syndrome (sequence analysis of MNX1 gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the MNX1 gene.
More info about this panel Portugal.
CURRARINO Syndrome Panel
Belgium.
By Centre de Genetique Humaine Institut de Pathologie et de Genetique
This panel specifically test the MNX1 gene.
More info about this panel Belgium.
Currarino Syndrome via MNX1 Gene Sequencing with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics
This panel specifically test the MNX1 gene.
More info about this panel United States.
Currarino syndrome Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the MNX1 gene.
More info about this panel Germany.
Currarino syndrome Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the MNX1 gene.
More info about this panel Austria.
qChip Panel
Spain.
By Quantitative Genomic Medicine Laboratories, SL qChip that also includes the following genes: RS1 RUNX2 SALL1 SCN1A BMPR1A SH2D1A SEM1 SHH SHOX SIM1
More info about this panel Spain.
Currarino syndrome Panel
Slovakia.
By MedGene
This panel specifically test the MNX1 gene.
More info about this panel Slovakia.
Currarino syndrome: MNX1(HLXB9) gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the MNX1 gene.
More info about this panel Spain.
MNX1 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the MNX1 gene.
More info about this panel United States.
Currarino triad Panel
Spain.
By Bioarray
This panel specifically test the MNX1 gene.
More info about this panel Spain.
Rapid microarray (CGH and SNP) Panel
United States.
By Allele Diagnostics Allele Diagnostics Rapid microarray (CGH and SNP) that also includes the following genes: RPS19 RUNX2 SALL1 SCN1A SCN2A SDHB SDHD BMPR1A SGCE SH2D1A
More info about this panel United States.
High-Resolution Rapid Microarray (CGH and SNP) Panel
United States.
By Allele Diagnostics Allele Diagnostics High-Resolution Rapid Microarray (CGH and SNP) that also includes the following genes: RPS19 RUNX2 SALL1 SCN1A SCN2A SDHB SDHD BMPR1A SGCE SH2D1A
More info about this panel United States.
Caris MI TumorSeek 592-Gene NGS Panel Panel
United States.
By Caris Life Sciences Caris MI TumorSeek 592-Gene NGS Panel that also includes the following genes: BCL6 BCL7A BCL9 BCR ROS1 RPL10 RPL22 RPL5 RPN1 RUNX1
More info about this panel United States.
Currarino syndrome Panel
Canada.
By LifeLabs Genetics
This panel specifically test the MNX1 gene.
More info about this panel Canada.
Currarino Syndrome, Sequencing MNX1 (HLXB9) Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the MNX1 gene.
More info about this panel Spain.
Currarino Syndrome, Deletions-Duplications (MLPA) MNX1 (HLXB9) Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the MNX1 gene.
More info about this panel Spain.
Tempus xO assay Panel
United States.
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
More info about this panel United States.
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like NPHP3-ACAD11 DAXX ACACA ABCD4 ELANE HNRNPU WDR81