Mental Retardation, Autosomal Recessive 56; Mrt56
Genes related to Mental Retardation, Autosomal Recessive 56; Mrt56
- ZC3H14
Clinical Features
Phenotypes and symptoms related to Mental Retardation, Autosomal Recessive 56; Mrt56
- Intellectual disability
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.Mental Retardation, Autosomal Recessive 56; Mrt56 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By Genetic Services Laboratory University of Chicago (United States).
RPS6KA3, CLIP1, SCN2A, ST3GAL3, SLC16A2, SLC25A1, SLC6A8, SLC9A6, SMARCA4, SMARCB1, ARID1A, SMC1A, KDM5C, SMS, SOX11, CDKL5, STXBP1, SYN1, SYNGAP1, SYP , (...)
View the complete list with 153 more genes
Specificity
1 %
Genes
100 % |
![]() By Genetic Services Laboratory University of Chicago (United States).
ST3GAL3, SLC25A1, STXBP1, VLDLR, ERLIN2, CA8, CNTNAP2, ARFGEF2, PCNT, L2HGDH, ZC3H14, VPS13B, ALG6, MED23, NSUN2, D2HGDH, DDHD2, ZNF526, C12orf57, CRBN , (...)
View the complete list with 16 more genes
Specificity
3 %
Genes
100 % |
![]() By PreventionGenetics PreventionGenetics (United States).
BDNF, RPS6KA3, SCN2A, SCN8A, SLC16A2, SLC2A1, SLC6A8, SLC9A6, SMC1A, KDM5C, STXBP1, TBR1, TCF4, TSPAN7, TRIO, UBA7, UBE2A, ZNF711, BCL11A, FTSJ1 , (...)
View the complete list with 90 more genes
Specificity
1 %
Genes
100 % |
![]() By Institute of Human Genetics Uniklinik RWTH Aachen (Germany).
RGS7, RIT1, RMRP, BCS1L, RPL10, RPS6KA3, RRAS, SALL1, SC5D, ATXN10, BLM, SCN1A, SCN2A, SCN8A, SCO2, AIMP1, SDCCAG8, SDHA, SDHB, SGSH , (...)
View the complete list with 845 more genes
Specificity
1 %
Genes
100 % |
![]() By Fulgent Genetics Fulgent Genetics (United States).
ZC3H14
Specificity
100 %
Genes
100 % |
![]() By Reference Laboratory Genetics (Spain).
RPS6KA3, ST3GAL3, SLC6A8, SMARCA4, SMARCB1, ARID1A, KDM5C, STXBP1, SYNGAP1, SYP, TAF2, TSPAN7, MED12, TRIO, VLDLR, ZBTB18, ZNF711, FTSJ1, ERLIN2, CA8 , (...)
View the complete list with 71 more genes
Specificity
2 %
Genes
100 % |
![]() By Reference Laboratory Genetics (Spain).
ST3GAL3, STXBP1, TAF2, VLDLR, ERLIN2, CA8, CNTNAP2, FMN2, ZC3H14, CRADD, MED23, NSUN2, TTI2, WASHC4, SOBP, CRBN, CC2D1A, TUSC3, TRAPPC9, LINS1 , (...)
View the complete list with 12 more genes
Specificity
4 %
Genes
100 % |
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Learn moreSources and references
You can check the following sources for additional information.
OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like POLYDACTYLY, POSTAXIAL, TYPE A1; PAPA1 POLYDACTYLY, POSTAXIAL, TYPE A7; PAPA7 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7 AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I, WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA; APS1 MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44 DEAFNESS, AUTOSOMAL RECESSIVE 98; DFNB98 GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE