Spermatogenic Failure 11; Spgf11

Clinical Features

Phenotypes and symptoms related to Spermatogenic Failure 11; Spgf11

  • Infertility
  • Abnormal sperm morphology

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Spermatogenic Failure 11; Spgf11 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Male Infertility Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

SEMA3A, SEMA3E, FOXL2, BRDT, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAR, AURKC, TAC3, TACR3, TAF4B, TEX11, WNT4, WT1, WWOX , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
100 %
Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

ROR2, SALL1, BMP15, BMP4, SEMA3A, SEMA3E, BMP7, FOXL2, BRDT, SOS1, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAG3, STAR, AURKC , (...)

View the complete list with 187 more genes
Specificity
1 %
Genes
100 %
KLHL10.

By Fulgent Genetics Fulgent Genetics (United States).

KLHL10
Specificity
100 %
Genes
100 %
Spermatogenic Failure , Panel Massive Sequencing (NGS) 9 Genes.

By Reference Laboratory Genetics (Spain).

AURKC, USP9Y, CATSPER1, SYCP3, KLHL10, DPY19L2, SEPT12, SPATA16, NR5A1
Specificity
12 %
Genes
100 %

You can get up to -4 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6 PSEUDOHYPOPARATHYROIDISM, TYPE IB; PHP1B DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1 AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1 CHAR SYNDROME; CHAR ABETAL34V AMYLOIDOSIS COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1