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NeoPainel for Inborn Errors of Metabolism

This panel analyzes a comprehensive set of genes associated with inborn errors of metabolism (IEM), including lysosomal and mitochondrial disorders and disorders of organic acids, amino acids, carbohydrates, lipids and other metabolic pathways.

Accepted samples
Peripheral blood (preferred), Buccal swab, Extracted DNA
Turnaround time and when it starts
Standard · 30 calendar days, after acceptance of the sample Fast · 15 calendar days, after acceptance of the sample
Medical order
Required. View requirements and limitations.

Test information

Technical details for NeoPainel for Inborn Errors of Metabolism

Method, scope, requirements and limitations

This panel analyzes a comprehensive set of genes associated with inborn errors of metabolism (IEM), including lysosomal and mitochondrial disorders and disorders of organic acids, amino acids, carbohydrates, lipids and other metabolic pathways.

Applications
Rare and hereditary diseases
Accepted samples
Peripheral blood (preferred), Buccal swab, Extracted DNA
Estimated turnaround time
Standard · 30 calendar days, after acceptance of the sample Fast · 15 calendar days, after acceptance of the sample
Sequencing method
Next-generation exome sequencing (NGS), with analysis targeted to the panel’s genes.
Analytical scope
Analysis of the listed genes, associated with inborn errors of metabolism, using exome data and the laboratory’s validated technical criteria.
Genes analyzed
763 genes analyzed.
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AARS2, AASS, ABAT, ABCA1, ABCB11, ABCB4, ABCB7, ABCD1, ABCD4, ABCG5, ABCG8, ABHD12, ABHD5, ACACA, ACAD8, ACAD9, ACADM, ACADS, ACADSB, ACADVL, ACAT1, ACO2, ACOX1, ACSF3, ACY1, ADA, ADAR, ADSL, AFG3L2, AGA, AGK, AGL, AGPS, AGXT, AHCY, AIFM1, AKR1D1, ALAD, ALAS2, ALDH18A1, ALDH3A2, ALDH4A1, ALDH5A1, ALDH6A1, ALDH7A1, ALDOA, ALDOB, ALG1, ALG11, ALG12, ALG14, ALG3, ALG6, ALG8, ALG9, ALPL, AMACR, AMN, AMT, ANO10, APOA1, APOA5, APOB, APOC2, APOE, APRT, APTX, ARG1, ARSA, ARSB, ARSG, ARSK, ARSL, ASAH1, ASL, ASPA, ASS1, ATAD3A, ATIC, ATP13A2, ATP5F1A, ATP5F1D, ATP5F1E, ATP5MC3, ATP5PO, ATP6AP1, ATP6V0A2, ATP7A, ATP7B, ATP8B1, ATPAF2, AUH, B3GALNT2, B3GALT6, B3GAT3, B3GLCT, B4GALNT1, B4GALT1, B4GALT7, BAAT, BCAT2, BCKDHA, BCKDHB, BCKDK, BCS1L, BOLA3, BTD, C19ORF12, C1QBP, CA5A, CARS2, CAT, CBLIF, CBS, CHCHD10, CHKB, CHST14, CHST3, CHST6, CHSY1, CISD2, CLDN16, CLDN19, CLN3, CLN5, CLN6, CLN8, CLPB, CLPP, CNNM2, COA6, COA7, COA8, COG1, COG4, COG5, COG6, COG7, COG8, COQ2, COQ4, COQ6, COQ7, COQ8A, COQ8B, COQ9, COX10, COX14, COX15, COX20, COX5A, COX6A1, COX6B1, COX7B, COXFA4, CP, CPOX, CPS1, CPT1A, CPT2, CREB3L3, CRLS1, CRPPA, CSGALNACT1, CTH, CTNS, CTSA, CTSC, CTSD, CTSF, CTSK, CUBN, CYC1, CYP27A1, CYP7B1, D2HGDH, DARS1, DARS2, DBH, DBT, DCXR, DDC, DDOST, DGUOK, DHCR24, DHCR7, DHFR, DHODH, DHRSX, DHTKD1, DLAT, DLD, DNA2, DNAJC12, DNAJC19, DNAJC5, DNM1L, DNM2, DOLK, DPAGT1, DPM1, DPM2, DPM3, DPYD, DPYS, DYM, EARS2, EBP, ECHS1, EDEM3, EHBP1L1, ELAC2, ENO3, EOGT, EPG5, EPM2A, ETFA, ETFB, ETFDH, ETHE1, EXT1, EXT2, FA2H, FAH, FARS2, FASTKD2, FBP1, FBXL4, FCSK, FDX2, FDXR, FECH, FGFR2, FH, FKRP, FKTN, FLAD1, FMO3, FOLR1, FOXRED1, FTCD, FUCA1, FUT8, FXN, G6PC1, G6PC3, GAA, GABRG2, GALC, GALE, GALK1, GALM, GALNS, GALNT2, GALNT3, GALT, GAMT, GARS1, GATM, GBA1, GBE1, GCDH, GCH1, GCLC, GCSH, GDAP1, GFER, GFM1, GFM2, GFPT1, GK, GLA, GLB1, GLDC, GLRA1, GLRX5, GLS, GLUD1, GLUL, GLYCTK, GM2A, GMPPA, GMPPB, GNE, GNMT, GNPAT, GNPTAB, GNPTG, GNS, GORAB, GPD1, GPHN, GPIHBP1, GRHPR, GRN, GSS, GSTZ1, GTPBP3, GUSB, GYG1, GYS1, GYS2, HAAO, HADH, HADHA, HADHB, HAMP, HARS2, HCCS, HCFC1, HEXA, HEXB, HFE, HGD, HGSNAT, HIBCH, HJV, HLCS, HMBS, HMGCL, HMGCS2, HOGA1, HPD, HPRT1, HPS1, HS2ST1, HSD17B10, HSD17B4, HSD3B7, HSPA9, HSPD1, HTRA2, HYAL1, IARS2, IBA57, IDH2, IDS, IDUA, IER3IP1, ISCA1, ISCA2, ISCU, ITPA, IVD, KARS1, KYNU, L2HGDH, LAMP2, LARGE1, LARS1, LARS2, LBR, LCAT, LCT, LDHA, LDLR, LDLRAP1, LETM1, LFNG, LIAS, LIPA, LIPT1, LIPT2, LMBRD1, LMF1, LONP1, LPIN1, LPL, LRPPRC, LYRM4, LYRM7, MAGT1, MAN1B1, MAN2B1, MANBA, MAOA, MARS2, MAT1A, MCCC1, MCCC2, MCEE, MCOLN1, MDH2, MECR, MFF, MFN2, MFSD8, MGAT2, MGME1, MICOS13, MICU1, MIPEP, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MMUT, MOCS1, MOCS2, MOGS, MPC1, MPDU1, MPI, MPV17, MRM2, MRPL3, MRPL44, MRPS2, MRPS22, MRPS34, MSMO1, MSTO1, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MTFMT, MTHFR, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MTO1, MTPAP, MTR, MTRFR, MT-RNR1, MTRR, MT-TA, MT-TC, MT-TD, MT-TE, MT-TF, MT-TG, MT-TH, MT-TI, MT-TK, MT-TL1, MT-TL2, MT-TM, MT-TN, MTTP, MT-TP, MT-TQ, MT-TR, MT-TS1, MT-TS2, MT-TT, MT-TV, MT-TW, MT-TY, MVK, NADK2, NAGA, NAGLU, NAGS, NARS2, NAXD, NAXE, NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA13, NDUFA2, NDUFA6, NDUFA8, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF3, NDUFAF4, NDUFAF5, NDUFAF6, NDUFAF8, NDUFB10, NDUFB11, NDUFB3, NDUFB8, NDUFC2, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NEU1, NFS1, NFU1, NGLY1, NHLRC1, NNT, NPC1, NPC2, NSDHL, NSUN3, NT5C3A, NT5E, NUBPL, NUS1, OAT, OCRL, OGDH, OPA1, OPA3, OTC, OXCT1, PAH, PANK2, PARS2, PC, PCBD1, PCCA, PCCB, PCK1, PCSK9, PDHA1, PDHB, PDHX, PDK3, PDP1, PDSS1, PDSS2, PEPD, PET100, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PFKM, PGAM2, PGAP2, PGAP3, PGK1, PGM1, PGM3, PHGDH, PHKA1, PHKA2, PHKB, PHKG2, PHYH, PIGA, PIGL, PIGM, PIGN, PIGO, PIGS, PIGT, PIGV, PIGW, PINK1, PLA2G6, PMM2, PMPCA, PMPCB, PNP, PNPLA2, PNPLA8, PNPO, PNPT1, POLG, POLG2, POMGNT1, POMGNT2, POMK, POMT1, POMT2, POR, PPA2, PPOX, PPT1, PRKAG2, PRODH, PRPS1, PSAP, PSAT1, PTCD3, PTS, PUS1, PYCR1, PYGL, PYGM, QDPR, QRSL1, RARS2, RBCK1, RBP4, RFT1, RMND1, RNASEH1, RNASEH2A, RNASEH2B, RNASEH2C, RPIA, RPL10, RRM2B, RTN4IP1, RXYLT1, SACS, SAMHD1, SAR1B, SARS2, SC5D, SCO1, SCO2, SCP2, SDHA, SDHAF1, SDHB, SDHD, SEC23B, SERAC1, SETX, SFXN4, SGSH, SHMT2, SI, SKIC2, SKIC3, SLC12A3, SLC13A3, SLC16A1, SLC17A5, SLC18A2, SLC19A2, SLC19A3, SLC22A5, SLC25A1, SLC25A12, SLC25A13, SLC25A15, SLC25A19, SLC25A20, SLC25A22, SLC25A26, SLC25A3, SLC25A32, SLC25A38, SLC25A4, SLC25A42, SLC25A46, SLC2A1, SLC2A2, SLC30A10, SLC35A1, SLC35A2, SLC35C1, SLC35D1, SLC37A4, SLC39A14, SLC39A4, SLC39A8, SLC3A1, SLC40A1, SLC46A1, SLC52A2, SLC52A3, SLC5A1, SLC5A6, SLC6A19, SLC6A3, SLC6A8, SLC7A7, SLC7A9, SMPD1, SPG7, SPR, SPTLC1, SPTLC2, SRD5A3, SSBP1, SSR4, ST3GAL3, ST3GAL5, STS, STT3A, SUCLA2, SUCLG1, SUMF1, SUOX, SURF1, TACO1, TAFAZZIN, TALDO1, TANGO2, TARS2, TAT, TCN2, TFAM, TFR2, TH, TIMM50, TIMM8A, TIMMDC1, TK2, TMEM126B, TMEM165, TMEM70, TOP3A, TPK1, TPP1, TRAP1, TREX1, TRIM37, TRIT1, TRMT10C, TRMT5, TRMU, TRNT1, TRPM6, TSFM, TTC19, TTPA, TUFM, TUSC3, TWNK, TYMP, UGT1A1, UMOD, UMPS, UPB1, UQCC2, UQCRB, UQCRC2, UQCRFS1, UROD, UROS, VARS2, VIPAS39, VKORC1, VMA12, VMA22, VPS16, VPS33A, VPS33B, WARS2, WDR45, WFS1, XDH, XPNPEP3, XYLT1, XYLT2, YARS2

Medical order
Required

Requirements

A medical order and sufficient clinical information to guide the analysis.

Limitations

The result depends on sample quality, achieved coverage and the method’s limitations. Variants outside the validated scope may not be detected.

Additional information

The gene list, scope and turnaround times reflect the current revision. Interpretation should take clinical information and, when indicated, genetic counseling into account.