SUGCT gene related symptoms and diseases
All the information presented here about the SUGCT gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,NCBIGENE,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to SUGCT gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Failure to thrive | Very Common - Between 80% and 100% cases |
| Hypertension | Very Common - Between 80% and 100% cases |
| Vomiting | Very Common - Between 80% and 100% cases |
| Diarrhea | Very Common - Between 80% and 100% cases |
| Acidosis | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with SUGCT gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Aciduria
- Goiter
- Abnormality of mitochondrial metabolism
- Hyperthyroidism
- Glutaric aciduria
- Glutaric acidemia
Rare diseases associated to SUGCT gene
Here you will find a list of rare diseases related to the SUGCT. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
GLUTARIC ACIDEMIA TYPE 3
Alternate names
GLUTARIC ACIDEMIA TYPE 3 Is also known as glutaryl-coa oxidase deficiency, ga iii, glutaric aciduria type 3
Description
Glutaryl-CoA oxidase deficiency is a peroxisomal disorder leading to glutaric aciduria. The prevalence is unknown. There is no distinctive phenotype associated with this disorder and one of the reported cases was asymptomatic. Transmission appears to be autosomal recessive.
Most common symptoms of GLUTARIC ACIDEMIA TYPE 3
- Failure to thrive
- Hypertension
- Vomiting
- Diarrhea
- Acidosis
More info about GLUTARIC ACIDEMIA TYPE 3
Search interest in SUGCT
Potential gene panels for SUGCT gene
C7orf10 Deletion/Duplication Analysis Panel
United States.
By Baylor Miraca Genetics Laboratories
This panel specifically test the SUGCT gene.
More info about this panel United States.
C7orf10 Familial Mutation/Variant Analysis Panel
United States.
By Baylor Miraca Genetics Laboratories
This panel specifically test the SUGCT gene.
More info about this panel United States.
C7orf10 Prenatal Sequence Analysis Panel
United States.
By Baylor Miraca Genetics Laboratories
This panel specifically test the SUGCT gene.
More info about this panel United States.
C7orf10 Sequence Analysis Panel
United States.
By Baylor Miraca Genetics Laboratories
This panel specifically test the SUGCT gene.
More info about this panel United States.
C7orf10 Sequence and Deletion/Duplication Analysis Panel
United States.
By Baylor Miraca Genetics Laboratories
This panel specifically test the SUGCT gene.
More info about this panel United States.
Glutaric Acidemia, Type 3 - C7ORF10 Sequencing Panel
United States.
By Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado
This panel specifically test the SUGCT gene.
More info about this panel United States.
Lysosomal and peroxisomal diseases (NGS panel of 109 genes) Panel
Portugal.
By CGC Genetics Lysosomal and peroxisomal diseases (NGS panel of 109 genes) that also includes the following genes: SC5D SCP2 SGSH SHOX SLC17A5 SMPD1 TCIRG1 ACOX1 ACP2 MCOLN1
More info about this panel Portugal.
Lysosomal and peroxisomal diseases (NGS panel of 109 genes) Panel
Portugal.
By CGC Genetics Lysosomal and peroxisomal diseases (NGS panel of 109 genes) that also includes the following genes: SC5D SCP2 SGSH SHOX SLC17A5 SMPD1 TCIRG1 ACOX1 ACP2 MCOLN1
More info about this panel Portugal.
CentoICU platinum plus Panel
Germany.
By Centogene AG - the Rare Disease Company CentoICU platinum plus that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC
More info about this panel Germany.
New Born testing (CentoICU) Panel
Germany.
By Centogene AG - the Rare Disease Company New Born testing (CentoICU) that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC
More info about this panel Germany.
Glutaric aciduria type 3 Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the SUGCT gene.
More info about this panel Germany.
C7orf10 Panel
Austria.
By Division Human Genetics Medical University Innsbruck
This panel specifically test the SUGCT gene.
More info about this panel Austria.
Nuclear-Mito NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Nuclear-Mito NGS Panel that also includes the following genes: RNASEL BCS1L RPL35A MRPL3 RYR1 RYR2 SACS ACSM3 SARDH ATXN7
More info about this panel United States.
SUGCT Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the SUGCT gene.
More info about this panel United States.
Organic Acidemia/Aciduria & Cobalamin Deficiency Panel Panel
Finland.
By Blueprint Genetics Organic Acidemia/Aciduria & Cobalamin Deficiency Panel that also includes the following genes: BCS1L SLC25A1 SUCLG1 TCN2 UMPS AMN CBS SUGCT CD320 MCEE
More info about this panel Finland.
Comprehensive Metabolism Panel Panel
Finland.
By Blueprint Genetics Comprehensive Metabolism Panel that also includes the following genes: BCS1L CNNM2 RYR1 CNNM4 SCN4A SEC23B SGSH SI SLC40A1 SLC12A3
More info about this panel Finland.
Peroxisomal Disorders Panel Panel
Finland.
By Blueprint Genetics Peroxisomal Disorders Panel that also includes the following genes: ACOX1 SUGCT DYM PEX26 EBP AGPS AGXT GNPAT AMACR HSD17B4
More info about this panel Finland.
GLUTARIC ACIDURIA NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL GLUTARIC ACIDURIA NGS PANEL that also includes the following genes: SUGCT ETFA ETFB ETFDH GCDH
More info about this panel Spain.
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