Spermatogenic Failure 7; Spgf7
Genes related to Spermatogenic Failure 7; Spgf7
- STRC
- CATSPER2
- CATSPER1
Clinical Features
Phenotypes and symptoms related to Spermatogenic Failure 7; Spgf7
- Infertility
- Male infertility
- Oligospermia
- Reduced sperm motility
- Nonmotile sperm
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.
Alternative names
Spermatogenic Failure 7; Spgf7 Is also known as miar, male infertility, nonsyndromic, autosomal recessive.
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 7; Spgf7 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Hearing Loss Advanced Sequencing and CNV Evaluation.
By Athena Diagnostics Inc (United States).
BCS1L, ROR1, SALL1, SEMA3E, SIX1, SIX5, SLC12A1, SLC19A2, SLC22A4, SNAI2, SMPX, SOX10, TBX1, TCOF1, TECTA, TFAP2A, TIMM8A, TJP2, TMPRSS3, USH1C , (...)
View the complete list with 149 more genes
Specificity
1 %
Genes
34 % |
OtoSCOPE.
By Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics (United States).
ROR1, SIX1, SIX5, SLC22A4, SNAI2, SMPX, SOX10, TBX1, TWNK, TCOF1, TECTA, TIMM8A, TJP2, TMPRSS3, USH1C, USH2A, CLRN1, TSPEAR, WFS1, ESPN , (...)
View the complete list with 130 more genes
Specificity
2 %
Genes
67 % |
Hearing Loss Panel.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
RPS6KA3, SALL1, SEMA3E, SIX1, SIX5, SLC19A2, SNAI2, SMPX, SOX10, BTD, TCOF1, TECTA, TIMM8A, TJP2, TMPRSS3, USH1C, USH2A, CLRN1, WFS1, ESPN , (...)
View the complete list with 100 more genes
Specificity
1 %
Genes
34 % |
OtoGenome Test for Hearing Loss (110 Genes).
By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine (United States).
BCS1L, SIX1, SNAI2, SMPX, SOX10, TECTA, TIMM8A, TMPRSS3, USH1C, USH2A, CLRN1, WFS1, ESPN, CLIC5, CDH23, CABP2, RIPOR2, CACNA1D, ACTG1, PCDH15 , (...)
View the complete list with 89 more genes
Specificity
2 %
Genes
67 % |
Expanded Hearing Loss Panel, Sequencing and Deletion/Duplication.
By ARUP Laboratories, Molecular Genetics and Genomics (United States).
SMPX, TECTA, TMPRSS3, USH1C, USH2A, CLRN1, WFS1, ESPN, CDH23, ACTG1, PCDH15, STRC, USH1G, WHRN, OTOA, TMC1, TRIOBP, ADGRV1, CCDC50, CLDN14 , (...)
View the complete list with 35 more genes
Specificity
2 %
Genes
34 % |
Audiome (hearing loss panel).
By Division of Genomic Diagnostics The Children's Hospital of Philadelphia (United States).
BCS1L, SIX1, SNAI2, SMPX, SOX10, SUCLA2, TECTA, TIMM8A, TMPRSS3, USH1C, USH2A, CLRN1, TSPEAR, WFS1, ESPN, CLIC5, CDH23, CABP2, PCDH15, OSBPL2 , (...)
View the complete list with 85 more genes
Specificity
1 %
Genes
34 % |
Deafness, autosomal recessive 16 (sequence analysis of STRC gene).
By CGC Genetics (Portugal).
STRC
Specificity
100 %
Genes
34 % |
Non syndromic deafness AR and XL (NGS panel for 56 genes).
By CGC Genetics (Portugal).
SLC12A1, SMPX, TECTA, TMPRSS3, USH1C, TSPEAR, ESPN, CLIC5, CDH23, CABP2, PCDH15, STRC, WHRN, OTOA, TMC1, TMC2, TRIOBP, GIPC3, CLDN14, LHFPL5 , (...)
View the complete list with 35 more genes
Specificity
2 %
Genes
34 % |
You can get up to 28 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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