KLHL10 gene related symptoms and diseases
All the information presented here about the KLHL10 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,ORPHANET,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to KLHL10 gene
Symptoms // Phenotype | % Cases |
---|---|
Infertility | Uncommon - Between 30% and 50% cases |
Abnormal sperm morphology | Uncommon - Between 30% and 50% cases |
Decreased testicular size | Uncommon - Between 30% and 50% cases |
Azoospermia | Uncommon - Between 30% and 50% cases |
Increased circulating gonadotropin level | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with KLHL10 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Abnormal spermatogenesis
- Obstructive azoospermia
- Non-obstructive azoospermia
Rare diseases associated to KLHL10 gene
Here you will find a list of rare diseases related to the KLHL10. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SPERMATOGENIC FAILURE 11; SPGF11
Most common symptoms of SPERMATOGENIC FAILURE 11; SPGF11
- Infertility
- Abnormal sperm morphology
More info about SPERMATOGENIC FAILURE 11; SPGF11
SOURCES: OMIM
MALE INFERTILITY WITH AZOOSPERMIA OR OLIGOZOOSPERMIA DUE TO SINGLE GENE MUTATION
Description
Male infertility with azoospermia or oligospermia due to single gene mutation is a rare, genetic male infertility due to sperm disorder characterized by the absence of a measurable amount of spermatozoa in the ejaculate (azoospermia), or a number of sperm in the ejaculate inferior to 15 million/mL (oligozoospermia), resulting from a mutation in a single gene known to cause azoo- or oligo-spermia. Sperm morphology may be normal.
Most common symptoms of MALE INFERTILITY WITH AZOOSPERMIA OR OLIGOZOOSPERMIA DUE TO SINGLE GENE MUTATION
- Decreased testicular size
- Azoospermia
- Increased circulating gonadotropin level
- Abnormal spermatogenesis
- Obstructive azoospermia
More info about MALE INFERTILITY WITH AZOOSPERMIA OR OLIGOZOOSPERMIA DUE TO SINGLE GENE MUTATION
SOURCES: ORPHANET
Search interest in KLHL10
Potential gene panels for KLHL10 gene
Male Infertility Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Male Infertility Sequencing Panel with CNV Detection that also includes the following genes: SEMA3A SEMA3E FOXL2 BRDT SOX10 SOX2 SOX3 SOX9 SRA1 SRD5A2
More info about this panelDisorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection that also includes the following genes: ROR2 SALL1 BMP15 BMP4 SEMA3A SEMA3E BMP7 FOXL2 BRDT SOS1
More info about this panelKLHL10 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the KLHL10 gene.
More info about this panelSpermatogenic Failure , Panel Massive Sequencing (NGS) 9 Genes Panel
By Reference Laboratory Genetics Spermatogenic Failure , Panel Massive Sequencing (NGS) 9 Genes that also includes the following genes: AURKC USP9Y CATSPER1 SYCP3 KLHL10 DPY19L2 SEPT12 SPATA16 NR5A1
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