Mental Retardation, X-linked 9; Mrx9

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

Nonsyndromic mental retardation.

Genes related to Mental Retardation, X-linked 9; Mrx9

FTSJ1

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Clinical Features

Top most frequent phenotypes and symptoms related to Mental Retardation, X-linked 9; Mrx9

Intellectual disability
Seizures
Global developmental delay
Cognitive impairment
Delayed speech and language development
Depressed nasal bridge
Intellectual disability, mild
Autism
Macrotia
Aggressive behavior

And another 6 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— The onset for some of the known clinical features related to this disease may vary, including infantile onset .

Alternative names

Mental Retardation, X-linked 9; Mrx9 Is also known as mental retardation, x-linked 44, mrx44.

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, X-linked 9; Mrx9 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
NGS XLID Panel. By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States). RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TAF1, TIMM8A, TSPAN7, MED12, UBE2A, USP9X, ZMYM3, ZNF41, ZNF711 , (...) View the complete list with 94 more genes Panel complete gene list RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TAF1, TIMM8A, TSPAN7, MED12, UBE2A, USP9X, ZMYM3, ZNF41, ZNF711, ZNF81, FTSJ1, HDAC8, NSDHL, PCDH19, NLGN4X, NLGN3, WDR13, ARHGEF9, CASK, MBTPS2, RAB39B, BRWD3, PORCN, ARX, PHF6, ATP6AP2, ZDHHC9, NAA10, THOC2, CNKSR2, CLCN4, ZDHHC15, UPF3B, CLIC2, PHF8, BCOR, ZC4H2, RAB40AL, CUL4B, OFD1, LAS1L, PTCHD1, FAAH2, DCX, ZCCHC12, MAGT1, DKC1, CCDC22, FRMPD4, DLG3, IQSEC2, SHROOM4, DMD, NEXMIF, SRPX2, HUWE1, EBP, EIF2S3, AGTR2, ACSL4, FANCB, FGD1, FLNA, FMR1, AFF2, GDI1, GK, GPC3, GRIA3, GSPT2, HSD17B10, HCCS, HCFC1, HPRT1, IDS, IGBP1, AP1S2, IL1RAPL1, ABCD1, KLF8, L1CAM, LAMP2, MAOA, ARHGEF6, MECP2, MID1, MTM1, NDP, NDUFA1, NHS, OCRL, OGT, OPHN1, OTC, PAK3, ATP7A, CDK16, AIFM1, ATRX, PLP1, PQBP1, PRPS1, RBM10 Specificity 1 % Genes 100 %
X-linked mental retardation 9. By Center for Human Genetics, Inc (United States). FTSJ1 Specificity 100 % Genes 100 %
X-Linked Intellectual Disabilities Deletion/Duplication. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TIMM8A, TSPAN7, MED12, UBE2A, ZNF711, FTSJ1, NSDHL, PCDH19, NLGN4X , (...) View the complete list with 68 more genes Panel complete gene list RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TIMM8A, TSPAN7, MED12, UBE2A, ZNF711, FTSJ1, NSDHL, PCDH19, NLGN4X, NLGN3, ARHGEF9, CASK, MBTPS2, RAB39B, BRWD3, PORCN, ARX, PHF6, ATP6AP2, ZDHHC9, NAA10, CNKSR2, ZDHHC15, UPF3B, CLIC2, PHF8, BCOR, CUL4B, OFD1, PTCHD1, DCX, DKC1, CCDC22, FRMPD4, DLG3, IQSEC2, SHROOM4, DMD, NEXMIF, HUWE1, ACSL4, FANCB, FGD1, FLNA, FMR1, AFF2, GDI1, GK, GPC3, GRIA3, HSD17B10, HCCS, HPRT1, IDS, IGBP1, AP1S2, IL1RAPL1, L1CAM, LAMP2, MAOA, MECP2, MID1, NDP, NDUFA1, NHS, OCRL, OPHN1, OTC, PAK3, ATP7A, PDHA1, ATRX, PGK1, PLP1, PQBP1, PRPS1, RBM10 Specificity 2 % Genes 100 %
X-linked Intellectual Disabilities Sequencing. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TIMM8A, TSPAN7, MED12, UBE2A, ZNF711, FTSJ1, NSDHL, PCDH19, NLGN4X , (...) View the complete list with 68 more genes Panel complete gene list RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TIMM8A, TSPAN7, MED12, UBE2A, ZNF711, FTSJ1, NSDHL, PCDH19, NLGN4X, NLGN3, ARHGEF9, CASK, MBTPS2, RAB39B, BRWD3, PORCN, ARX, PHF6, ATP6AP2, ZDHHC9, NAA10, CNKSR2, ZDHHC15, UPF3B, CLIC2, PHF8, BCOR, CUL4B, OFD1, PTCHD1, DCX, DKC1, CCDC22, FRMPD4, DLG3, IQSEC2, SHROOM4, DMD, NEXMIF, HUWE1, ACSL4, FANCB, FGD1, FLNA, FMR1, AFF2, GDI1, GK, GPC3, GRIA3, HSD17B10, HCCS, HPRT1, IDS, IGBP1, AP1S2, IL1RAPL1, L1CAM, LAMP2, MAOA, MECP2, MID1, NDP, NDUFA1, NHS, OCRL, OPHN1, OTC, PAK3, ATP7A, PDHA1, ATRX, PGK1, PLP1, PQBP1, PRPS1, RBM10 Specificity 2 % Genes 100 %
X-Linked Intellectual Disabilities Sequencing and Deletion/Duplication. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TIMM8A, TSPAN7, MED12, UBE2A, ZNF711, FTSJ1, NSDHL, PCDH19, NLGN4X , (...) View the complete list with 67 more genes Panel complete gene list RPL10, RPS6KA3, SLC16A2, SLC9A6, SMC1A, KDM5C, SMS, SOX3, CDKL5, SYN1, SYP, TIMM8A, TSPAN7, MED12, UBE2A, ZNF711, FTSJ1, NSDHL, PCDH19, NLGN4X, NLGN3, ARHGEF9, CASK, MBTPS2, RAB39B, BRWD3, PORCN, ARX, PHF6, ATP6AP2, ZDHHC9, NAA10, CNKSR2, ZDHHC15, UPF3B, CLIC2, PHF8, BCOR, CUL4B, OFD1, PTCHD1, DCX, DKC1, CCDC22, FRMPD4, DLG3, IQSEC2, SHROOM4, DMD, NEXMIF, HUWE1, FANCB, FGD1, FLNA, FMR1, AFF2, GDI1, GK, GPC3, GRIA3, HSD17B10, HCCS, HPRT1, IDS, IGBP1, AP1S2, IL1RAPL1, L1CAM, LAMP2, MAOA, MECP2, MID1, NDP, NDUFA1, NHS, OCRL, OPHN1, OTC, PAK3, ATP7A, PDHA1, ATRX, PGK1, PLP1, PQBP1, PRPS1, RBM10 Specificity 2 % Genes 100 %
Non-Specific Intellectual Disability Panel. 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 Panel complete gene list RPS6KA3, CLIP1, SCN2A, ST3GAL3, SLC16A2, SLC25A1, SLC6A8, SLC9A6, SMARCA4, SMARCB1, ARID1A, SMC1A, KDM5C, SMS, SOX11, CDKL5, STXBP1, SYN1, SYNGAP1, SYP, TAF2, TCF4, TSPAN7, MED12, UBE2A, UBE3A, EZR, VLDLR, ZNF41, ZNF711, ZNF81, FTSJ1, KIF4A, NSDHL, ERLIN2, CTCF, CA8, CNTNAP2, CACNG2, FMN2, PCDH19, NLGN4X, NLGN3, SHANK3, SHANK2, ARHGEF9, DEAF1, ZEB2, CASK, ADNP, PCNT, RAB39B, FBXO31, ZMYND11, BRWD3, CDH15, ZNF674, ARID1B, ARX, PHF6, ATP6AP2, ZDHHC9, NAA10, ZNF407, ZDHHC15, UPF3B, MBD5, L2HGDH, ZC3H14, CLIC2, PHF8, TUBA1A, BCOR, VPS13B, ALG6, KIRREL3, CRADD, MED23, EHMT1, CTNNB1, ADAT3, CUL4B, SETD5, OFD1, PGAP1, NSUN2, TTI2, PTCHD1, METTL23, DCX, D2HGDH, MAGT1, CCDC22, FRMPD4, DLG3, IQSEC2, DDHD2, WASHC4, SHROOM4, SOBP, ZNF526, NEXMIF, C12orf57, DYNC1H1, DNMT3A, PACS1, CRBN, CC2D1A, TUSC3, SRPX2, GATAD2B, TRAPPC9, HUWE1, DYRK1A, LINS1, SLC6A17, EIF2S3, EPB41L1, AGTR2, ACSL4, FLNA, FMR1, AFF2, FOXG1, FOXP1, ALDH5A1, GDI1, TECR, GRIA3, GRIK2, GRIN1, GRIN2A, GRIN2B, HSD17B10, HCFC1, ANK3, HPRT1, IDH2, IGBP1, AP1S2, AP4B1, AP4E1, AP4M1, AP4S1, IL1RAPL1, KCNJ10, KLF8, KPTN, L1CAM, LRP2, MAN1B1, MAOA, ARHGEF6, MECP2, MEF2C, MID1, MID2, NDST1, NHS, NRXN1, NRXN2, OCRL, OPHN1, PAK3, PDHA1, ATRX, KIF1A, PLP1, PQBP1, PRPS1, PRSS12, PURA, RAI1 Specificity 1 % Genes 100 %
X-linked Non-Specific Intellectual Disability Panel. By Genetic Services Laboratory University of Chicago (United States). RPL10, RPS6KA3, SLC16A2, SLC6A8, SLC9A6, SMC1A, KDM5C, SMS, CDKL5, SYN1, SYP, TSPAN7, MED12, UBE2A, ZNF41, ZNF711, ZNF81, FTSJ1, NSDHL, PCDH19 , (...) View the complete list with 59 more genes Panel complete gene list RPL10, RPS6KA3, SLC16A2, SLC6A8, SLC9A6, SMC1A, KDM5C, SMS, CDKL5, SYN1, SYP, TSPAN7, MED12, UBE2A, ZNF41, ZNF711, ZNF81, FTSJ1, NSDHL, PCDH19, NLGN4X, NLGN3, ARHGEF9, CASK, RAB39B, BRWD3, ZNF674, ARX, PHF6, ATP6AP2, ZDHHC9, NAA10, ZDHHC15, UPF3B, CLIC2, PHF8, BCOR, CUL4B, OFD1, PTCHD1, DCX, MAGT1, CCDC22, FRMPD4, DLG3, IQSEC2, SHROOM4, NEXMIF, SRPX2, HUWE1, EIF2S3, AGTR2, ACSL4, FLNA, FMR1, AFF2, GDI1, GRIA3, HSD17B10, HCFC1, HPRT1, IGBP1, AP1S2, IL1RAPL1, KLF8, L1CAM, MAOA, ARHGEF6, MECP2, MID1, NHS, OCRL, OPHN1, PAK3, PDHA1, ATRX, PLP1, PQBP1, PRPS1 Specificity 2 % Genes 100 %
CustomNext: Neuro. By Ambry Genetics (United States). RPL10, RPS6KA3, SCN1A, SCN1B, SCN2A, SCN8A, ST3GAL3, SLC16A2, SLC2A1, SLC35A2, SLC6A1, SLC6A8, SLC9A6, SMARCA2, SMARCA4, SMARCB1, SMC1A, KDM5C, SMS, SNAP25 , (...) View the complete list with 176 more genes Panel complete gene list RPL10, RPS6KA3, SCN1A, SCN1B, SCN2A, SCN8A, ST3GAL3, SLC16A2, SLC2A1, SLC35A2, SLC6A1, SLC6A8, SLC9A6, SMARCA2, SMARCA4, SMARCB1, SMC1A, KDM5C, SMS, SNAP25, SIK1, SPTAN1, CDKL5, STXBP1, SYN1, SYNGAP1, TBR1, TCF4, TIMM8A, MED12, TSC1, TSC2, UBE2A, UBE3A, KAT6A, FTSJ1, HDAC8, CTCF, CA8, CNTNAP2, FOXP2, CACNA1A, CACNA1C, NSD1, PCDH19, NLGN4X, NLGN3, SHANK3, ARHGEF9, ZEB2, CASK, ADNP, PLCB1, DNAJC5, RAB39B, SCARB2, PRICKLE1, BRWD3, PORCN, ARID1B, ARX, PHF6, DEPDC5, STX1B, POGZ, KCNT1, CHD2, CHRNA2, CHRNA4, CHRNB2, SLC25A22, CHD8, UPF3B, MBD5, CHD7, PHF8, TPP1, CLN3, CLN5, CLN6, CLN8, ANKRD11, NHLRC1, SATB2, VPS13B, KCTD7, SLC13A5, CREBBP, CRH, MED23, EHMT1, SMC3, CSTB, ZC4H2, CTSD, CTSF, KATNAL2, CUL4B, OFD1, NSUN2, PTCHD1, DCX, DDX3X, MFSD8, DHCR7, NIPBL, WDR45, DLG3, SZT2, IQSEC2, TBC1D24, NEXMIF, TBL1XR1, DYNC1H1, DNM1, PACS1, ATP13A2, CC2D1A, TUSC3, PNPO, PRRT2, TRAPPC9, ALG13, HUWE1, DYRK1A, LINS1, EEF1A2, EPM2A, ACSL4, FGD1, FLNA, FMR1, FOLR1, FOXG1, FOXP1, GABRA1, GABRB3, GABRG2, GAMT, GATM, GDI1, GNAO1, GOSR2, GPC3, GRIA3, GRIN1, GRIN2A, GRIN2B, GRN, HCN1, HNRNPU, HOXA1, HPRT1, IDS, AP1S2, AP4B1, ABCD1, KCNA2, KCNC1, KCNJ10, KCNQ2, KCNQ3, L1CAM, LAMP2, LGI1, MAN1B1, MAOA, MECP2, MEF2C, MID1, NDP, NDUFA1, NHS, ATP1A2, NRXN1, OCRL, OPHN1, OTC, PAK3, ATP7A, ALDH7A1, PDHA1, ATRX, KIF1A, PIGA, PIGN, PLP1, PNKP, POLG, PPT1, PQBP1, PTEN, PTPN11, PURA, RAD21, RAI1 Specificity 1 % Genes 100 %

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Sources and references

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MESH OMIM Rare Disease Symptoms Checker

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