{"id":27675,"date":"2025-06-24T16:48:29","date_gmt":"2025-06-24T13:48:29","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/panel-erori-inascute-de-metabolism-centoiem\/"},"modified":"2026-07-02T11:30:59","modified_gmt":"2026-07-02T08:30:59","slug":"panel-erori-inascute-de-metabolism-centoiem","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-diagnostic-genetic\/panel-erori-inascute-de-metabolism-centoiem\/","title":{"rendered":"Panel erori inascute de metabolism &#8211; CentoIEM"},"content":{"rendered":"<p>Erorile \u00eenn\u0103scute de metabolism (Inborn Errors of Metabolism \u2013 IEM) reprezint\u0103 un grup heterogen de boli genetice cauzate de defecte enzimatice sau de transport implicate \u00een procesele metabolice esen\u021biale ale organismului. Acestea pot afecta metabolismul energetic, degradarea \u0219i sinteza aminoacizilor, lipidelor, carbohidra\u021bilor, acizilor organici, metabolismul mitocondrial, lizozomal \u0219i peroxizomal.<\/p>\n<p>Acest panel extins CentoIEM permite identificarea variantelor patogenice implicate \u00een forme severe, multisistemice sau cu debut neonatal, pediatric sau chiar adult al bolilor metabolice rare.<\/p>\n<h3>Tipuri de procese evaluate<\/h3>\n<h3>Panelul acoper\u0103 gene implicate \u00een:<\/h3>\n<ul>\n<li>metabolismul aminoacizilor \u0219i ureei<\/li>\n<li>beta-oxidarea acizilor gra\u0219i \u0219i metabolismul lipidic<\/li>\n<li>ciclul Krebs \u0219i produc\u021bia de energie mitocondrial\u0103<\/li>\n<li>lan\u021bul respirator mitocondrial<\/li>\n<li>metabolismul lizozomal \u0219i peroxizomal<\/li>\n<li>glicozilare \u0219i sintez\u0103 proteic\u0103<\/li>\n<li>transport membranar \u0219i homeostazie ionic\u0103<\/li>\n<li>metabolismul purinelor \u0219i pirimidinelor<\/li>\n<li>procese neurodegenerative metabolice<\/li>\n<\/ul>\n<h3>Afec\u021biuni sau simptome asociate<\/h3>\n<ul>\n<li>hipoglicemie recurent\u0103 sau sever\u0103<\/li>\n<li>acidoz\u0103 metabolic\u0103<\/li>\n<li>encefalopatie acut\u0103 sau cronic\u0103<\/li>\n<li>convulsii inexplicabile<\/li>\n<li>retard de dezvoltare psihomotorie<\/li>\n<li>hepatomegalie \/ insuficien\u021b\u0103 hepatic\u0103<\/li>\n<li>miopatie, fatigabilitate sever\u0103<\/li>\n<li>cardiomiopatie metabolic\u0103<\/li>\n<li>tulbur\u0103ri neurologice progresive<\/li>\n<li>acidoz\u0103 lactic\u0103 persistent\u0103<\/li>\n<li>episoade de decompensare metabolic\u0103<\/li>\n<li>afectare multisistemic\u0103 neonatal\u0103 sau infantil\u0103<\/li>\n<\/ul>\n<h3>Cui se adreseaz\u0103<\/h3>\n<ul>\n<li>nou-n\u0103scu\u021bilor cu suspiciune de boal\u0103 metabolic\u0103<\/li>\n<li>copiilor cu retard de dezvoltare \u0219i simptome neurologice inexplicabile<\/li>\n<li>pacien\u021bilor cu episoade recurente de decompensare metabolic\u0103<\/li>\n<li>adul\u021bilor cu suspiciune de boal\u0103 metabolic\u0103 latent\u0103 sau atipic\u0103<\/li>\n<li>cazurilor de encefalopatie f\u0103r\u0103 cauz\u0103 clar\u0103<\/li>\n<li>clinicienilor care doresc confirmare genetic\u0103 \u0219i consiliere familial\u0103<\/li>\n<\/ul>\n<h3>Metodologie de testare<\/h3>\n<ul>\n<li>secven\u021biere NGS (Next Generation Sequencing)<\/li>\n<li>analiz\u0103 complet\u0103 exon-intron pentru genele incluse<\/li>\n<li>detectarea variantelor punctiforme, dele\u021biilor \u0219i inser\u021biilor<\/li>\n<li>analiz\u0103 bioinformatic\u0103 avansat\u0103 \u0219i interpretare clinic\u0103 a variantelor<\/li>\n<li>raportare conform ghidurilor interna\u021bionale de genetic\u0103 medical\u0103<\/li>\n<\/ul>\n<h3>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/h3>\n<ul>\n<li>identific\u0103 etiologia genetic\u0103 a bolilor metabolice rare<\/li>\n<li>permite diagnostic precoce \u00eenainte de deteriorare ireversibil\u0103<\/li>\n<li>faciliteaz\u0103 tratament \u021bintit (dietetic, enzimatic sau farmacologic)<\/li>\n<li>reduce timpul p\u00e2n\u0103 la diagnostic \u00een cazuri complexe<\/li>\n<li>permite consiliere genetic\u0103 familial\u0103 \u0219i screening familial<\/li>\n<li>diferen\u021biaz\u0103 bolile metabolice de cele neurologice sau hepatice dob\u00e2ndite<\/li>\n<\/ul>\n<h3>Particularit\u0103\u021bi \u0219i limit\u0103ri<\/h3>\n<ul>\n<li>nu detecteaz\u0103 cauze non-genetice (toxice, infec\u021bioase, nutri\u021bionale)<\/li>\n<li>nu exclude complet existen\u021ba altor gene neincluse \u00een panel<\/li>\n<li>pot ap\u0103rea variante cu semnifica\u021bie incert\u0103 (VUS)<\/li>\n<li>rezultatele trebuie corelate strict cu datele clinice \u0219i biochimice<\/li>\n<\/ul>\n<h3>Tip de prob\u0103<\/h3>\n<p>s\u00e2nge periferic (EDTA) \u2013 <strong>2 \u00d7 6 ml<\/strong><\/p>\n<h3>Recoltare \u0219i condi\u021bii<\/h3>\n<ul>\n<li>recoltare \u00een vacutainer EDTA<\/li>\n<li>nu necesit\u0103 condi\u021bii de post alimentar<\/li>\n<\/ul>\n<h3>Denumiri alternative<\/h3>\n<ul>\n<li>Panel genetic erori \u00eenn\u0103scute de metabolism<\/li>\n<li>Test NGS boli metabolice rare<\/li>\n<li>Screening genetic metabolic extins CentoIEM<\/li>\n<li>Panel boli metabolice ereditare multisistemice<\/li>\n<li>Test genetic pentru tulbur\u0103ri metabolice congenitale<\/li>\n<\/ul>\n<h3>Analize asociate recomandate<\/h3>\n<ul>\n<li>profil metabolic seric \u0219i urinar (aminoacizi, acizi organici)<\/li>\n<li>lactat \u0219i piruvat<\/li>\n<li>amoniac plasmatic<\/li>\n<li>teste hepatice \u0219i renale extinse<\/li>\n<li>profil acilcarnitine<\/li>\n<li>imagistic\u0103 cerebral\u0103 (IRM)<\/li>\n<li>consult neurologic \u0219i metabolic<\/li>\n<li>consiliere genetic\u0103 pre \u0219i post testare<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Panelul analizeaz\u0103 un num\u0103r foarte extins de gene asociate cu erori \u00eenn\u0103scute de metabolism, incluz\u00e2nd tulbur\u0103ri ale metabolismului aminoacizilor, acizilor organici, acizilor gra\u0219i, metabolismului mitocondrial, lizozomal, peroxizomal, precum \u0219i defecte ale ciclului ureei, glicozil\u0103rii \u0219i metabolismului energetic celular. Testul permite identificarea cauzelor genetice ale unor boli metabolice rare, severe sau cu debut precoce.<\/p>\n<h3>Gene analizate<\/h3>\n<p>AARS2, ABCA1, ABCB4, ABCC2, ABCC8, ABCD1, ABCD4, ABCG5, ABCG8, ACAD8, ACAD9, ACADM, ACADS, ACADSB, ACADVL, ACAT1, ACOX1, ACSF3, ACY1, ADA, ADAMTS10, ADAMTSL2, ADAR, ADGRG1, ADK, ADSL, AFG3L2, AGA, AGL, AGPAT2, AGPS, AGXT, AHCY, AIFM1, AIMP1, AIMP2, AKT2, AKT3, ALAD, ALAS2, ALDH18A1, ALDH3A2, ALDH4A1, ALDH5A1, ALDH7A1, ALDOA, ALDOB, ALG1, ALG11, ALG12, ALG13, ALG2, ALG3, ALG6, ALG8, ALG9, ALPL, ALS2, AMN, AMPD2, AMT, ANK1, ANTXR2, AP3B1, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, APOA2, APOA5, APOB, APOC2, APOE, APP, APPL1, APTX, AQP2, ARG1, ARL6IP1, ARSA, ARSB, ASAH1, ASL, ASPA, ASS1, ATM, ATP13A2, ATP6V0A2, ATP7A, ATP7B, ATPAF2, ATRX, AUH, AVP, AVPR2, B3GALNT2, B4GALNT1, B4GALT1, BCAP31, BCKDHA, BCKDHB, BCS1L, BEST1, BICD2, BLK, BMP6, BOLA3, BRAT1, BSCL2, BTD, C19orf12, CA5A, CACNA1D, CAPN1, CASP10, CASP8, CAV1, CAVIN1, CBLIF, CBS, CCT5, CD320, CEL, CERS1, CETP, CISD2, CLCN2, CLN3, CLN5, CLN6, CLN8, CLPB, CLPP, COA7, COA8, COASY, COG1, COG4, COG5, COG6, COG7, COG8, COL11A2, COL2A1, COL4A1, COL4A2, COLGALT1, COQ2, COQ8A, COQ9, COX10, COX15, COX20, COX6B1, CP, CPOX, CPS1, CPT1A, CPT1C, CPT2, CSF1R, CTC1, CTH, CTLA4, CTNS, CTSA, CTSC, CTSD, CTSF, CTSK, CUBN, CYP11B1, CYP17A1, CYP19A1, CYP27A1, CYP2U1, CYP7B1, D2HGDH, DAG1, DARS1, DARS2, DBT, DCAF17, DDC, DDHD1, DDHD2, DDOST, DGUOK, DHCR7, DHDDS, DIABLO, DKC1, DLAT, DLD, DLL3, DNAJC5, DNM1L, DOLK, DPM1, DPM2, DPM3, DPYD, DSTYK, DYM, EARS2, ECHS1, EIF2AK3, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF2S3, ENO3, ENPP1, ENTPD1, EPB42, EPHX2, EPM2A, EPRS1, ERCC6, ERCC8, ERLIN1, ERLIN2, ETFA, ETFB, ETFDH, ETHE1, EXOSC3, F2, F5, FA2H, FADD, FAH, FARS2, FARSB, FAS, FASLG, FASTKD2, FBN1, FBP1, FBXL4, FDX2, FECH, FGF23, FH, FHL1, FLAD1, FOLR1, FOXA2, FOXP3, FOXRED1, FTL, FUCA1, G6PC1, G6PD, GAA, GABRB2, GALC, GALE, GALK1, GALNS, GALT, GAMT, GAN, GATA4, GATA6, GATM, GBA1, GBA2, GBE1, GCDH, GCK, GCSH, GFAP, GFER, GFM1, GFM2, GFPT1, GHR, GJA1, GJB1, GJC2, GK, GLA, GLB1, GLDC, GLIS3, GLRX5, GLUD1, GLUL, GM2A, GMPPA, GNE, GNMT, GNPAT, GNPTAB, GNPTG, GNS, GOSR2, GPC3, GRN, GTPBP2, GTPBP3, GUSB, GYG1, GYS1, GYS2, HACE1, HADH, HADHA, HADHB, HAMP, HCFC1, HEPACAM, HEXA, HEXB, HFE, HGD, HGSNAT, HIBCH, HIKESHI, HJV, HK1, HLCS, HMBS, HMGCL, HMGCS2, HNF1A, HNF1B, HNF4A, HPD, HPRT1, HRAS, HSD17B10, HSD17B4, HSD3B2, HSPD1, HTRA1, HYAL1, HYCC1, IARS2, IBA57, IDS, IDUA, IER3IP1, IFIH1, IL2RA, INS, INSR, ISCA2, ITIH4, ITK, IVD, JAG1, JAM3, KCNC1, KCNJ10, KCNJ11, KCNT1, KCTD7, KDM6A, KHK, KIDINS220, KIF1A, KIF1C, KIF5A, KLF11, KMT2D, KRAS, L1CAM, L2HGDH, LAMA2, LAMB1, LAMP2, LARGE1, LAT, LCAT, LDB3, LDHA, LDLR, LDLRAP1, LIAS, LIPA, LIPC, LIPE, LIPI, LIPT1, LIPT2, LMBRD1, LMNA, LMNB1, LPIN1, LPL, LRBA, LRPPRC, LYRM7, LYST, MAG, MAGT1, MAN1B1, MAN2B1, MANBA, MARS1, MARS2, MCCC1, MCCC2, MCEE, MCOLN1, MECR, MFSD8, MGAT2, MGME1, MLC1, MLPH, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MMUT, MOCS1, MOCS2, MOGS, MPDU1, MPI, MPV17, MRPL44, MRPS22, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-RNR1, MT-RNR2, 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, MT-TP, MT-TQ, MT-TR, MT-TS1, MT-TS2, MT-TT, MT-TV, MT-TW, MT-TY, MTFMT, MTHFR, MTPAP, MTR, MTRFR, MTRR, MYO5A, MYOT, NAGA, NAGLU, NAGS, NARS2, NAXD, NAXE, NBAS, NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA2, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF4, NDUFAF5, NDUFAF6, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NEU1, NEUROD1, NEUROG3, NFE2L2, NFU1, NGLY1, NHLRC1, NIPA1, NKX2-2, NKX6-2, NOTCH3, NPC1, NPC2, NPR2, NRAS, NT5C2, NUBPL, OAT, OCLN, OCRL, OPA3, OSGEP, OTC, OXCT1, PAH, PANK2, PAX4, PC, PCCA, PCCB, PCK1, PCSK9, PCYT2, PDHA1, PDHB, PDHX, PDP1, PDSS1, PDSS2, PDX1, PEPD, PET100, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PFKM, PGAM2, PGAP1, PGK1, PGM1, PHKA1, PHKA2, PHKB, PHKG2, PHYH, PIK3R1, PKLR, PLA2G6, PLAA, PLCG2, PLIN1, PLP1, PLPBP, PMM2, PMPCB, PNPLA6, PNPO, PNPT1, POLG, POLR1C, POLR3A, POLR3B, POR, PPARG, PPOX, PPP1R17, PPT1, PRF1, PRICKLE1, PRKAG2, PRKCD, PRODH, PSAP, PSEN1, PTF1A, PTS, PYCR2, PYGL, PYGM, QDPR, RAB11B, RAB27A, RAB3GAP2, RAI1, RARS1, RARS2, RBCK1, REEP1, REEP2, RFT1, RFX6, RNASEH2A, RNASEH2B, RNASEH2C, RNASET2, RNF216, RPIA, RRM2B, RTN2, SACS, SAMHD1, SCARB2, SCO1, SCO2, SDHA, SDHAF1, SDHB, SDHD, SERAC1, SERPINI1, SGSH, SI, SLC13A3, SLC16A1, SLC16A2, SLC17A5, SLC19A2, SLC19A3, SLC1A4, SLC22A5, SLC25A1, SLC25A12, SLC25A13, SLC25A15, SLC25A20, SLC25A4, SLC25A46, SLC2A1, SLC2A2, SLC33A1, SLC35A1, SLC35A2, SLC35C1, SLC3A1, SLC40A1, SLC4A1, SLC6A19, SLC6A8, SLC6A9, SLC7A7, SLC7A9, SLCO1B1, SLCO1B3, SMPD1, SNTA1, SOX10, SPART, SPAST, SPG11, SPG21, SPG7, SPTA1, SPTB, SRD5A3, SSR4, STAT1, STAT3, STT3A, STT3B, STX11, STXBP2, SUCLA2, SUCLG1, SUGCT, SUMF1, SUOX, SURF1, SYNE1, TACO1, TAFAZZIN, TAT, TBC1D24, TCF4, TCN2, TECPR2, TFG, TFR2, TGFB1, TINF2, TK2, TMEM106B, TMEM165, TMEM70, TPK1, TPP1, TREM2, TREX1, TRMT10A, TRPV4, TSFM, TTC19, TUBB4A, TUFM, TUSC3, TWNK, TYMP, TYROBP, UBAP1, UCHL1, UCP2, UFM1, UGT1A1, UMPS, UNC13D, UNC80, UQCRQ, UROD, UROS, USH1C, VAMP1, VCP, VPS11, VPS37A, WARS2, WASHC5, WDR45, WDR45B, WFS1, ZFP57, ZFYVE26, ZFYVE27<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,3166,2876],"product_tag":[],"class_list":["post-27675","product","type-product","status-publish","product_cat-analize","product_cat-diagnostic-genetic","product_cat-serviciu-laborator","first","instock","sale","virtual","purchasable","product-type-simple"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 5.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"CentoIEM - panel genetic pentru boli metabolice ereditare, recomandat \u00een suspiciune de tulbur\u0103ri metabolice, 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CLCN2, CLN3, CLN5, CLN6, CLN8, CLPB, CLPP, COA7, COA8, COASY, COG1, COG4, COG5, COG6, COG7, COG8, COL11A2, COL2A1, COL4A1, COL4A2, COLGALT1, COQ2, COQ8A, COQ9, COX10, COX15, COX20, COX6B1, CP, CPOX, CPS1, CPT1A, CPT1C, CPT2, CSF1R, CTC1, CTH, CTLA4, CTNS, CTSA, CTSC, CTSD, CTSF, CTSK, CUBN, CYP11B1, CYP17A1, CYP19A1, CYP27A1, CYP2U1, CYP7B1, D2HGDH, DAG1, DARS1, DARS2, DBT, DCAF17, DDC, DDHD1, DDHD2, DDOST, DGUOK, DHCR7, DHDDS, DIABLO, DKC1, DLAT, DLD, DLL3, DNAJC5, DNM1L, DOLK, DPM1, DPM2, DPM3, DPYD, DSTYK, DYM, EARS2, ECHS1, EIF2AK3, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF2S3, ENO3, ENPP1, ENTPD1, EPB42, EPHX2, EPM2A, EPRS1, ERCC6, ERCC8, ERLIN1, ERLIN2, ETFA, ETFB, ETFDH, ETHE1, EXOSC3, F2, F5, FA2H, FADD, FAH, FARS2, FARSB, FAS, FASLG, FASTKD2, FBN1, FBP1, FBXL4, FDX2, FECH, FGF23, FH, FHL1, FLAD1, FOLR1, FOXA2, FOXP3, FOXRED1, FTL, FUCA1, G6PC1, G6PD, GAA, GABRB2, GALC, GALE, GALK1, GALNS, GALT, GAMT, GAN, GATA4, GATA6, GATM, GBA1, GBA2, GBE1, GCDH, GCK, GCSH, GFAP, GFER, GFM1, GFM2, GFPT1, GHR, GJA1, GJB1, GJC2, GK, GLA, GLB1, GLDC, GLIS3, GLRX5, GLUD1, GLUL, GM2A, GMPPA, GNE, GNMT, GNPAT, GNPTAB, GNPTG, GNS, GOSR2, GPC3, GRN, GTPBP2, GTPBP3, GUSB, GYG1, GYS1, GYS2, HACE1, HADH, HADHA, HADHB, HAMP, HCFC1, HEPACAM, HEXA, HEXB, HFE, HGD, HGSNAT, HIBCH, HIKESHI, HJV, HK1, HLCS, HMBS, HMGCL, HMGCS2, HNF1A, HNF1B, HNF4A, HPD, HPRT1, HRAS, HSD17B10, HSD17B4, HSD3B2, HSPD1, HTRA1, HYAL1, HYCC1, IARS2, IBA57, IDS, IDUA, IER3IP1, IFIH1, IL2RA, INS, INSR, ISCA2, ITIH4, ITK, IVD, JAG1, JAM3, KCNC1, KCNJ10, KCNJ11, KCNT1, KCTD7, KDM6A, KHK, KIDINS220, KIF1A, KIF1C, KIF5A, KLF11, KMT2D, KRAS, L1CAM, L2HGDH, LAMA2, LAMB1, LAMP2, LARGE1, LAT, LCAT, LDB3, LDHA, LDLR, LDLRAP1, LIAS, LIPA, LIPC, LIPE, LIPI, LIPT1, LIPT2, LMBRD1, LMNA, LMNB1, LPIN1, LPL, LRBA, LRPPRC, LYRM7, LYST, MAG, MAGT1, MAN1B1, MAN2B1, MANBA, MARS1, MARS2, MCCC1, MCCC2, MCEE, MCOLN1, MECR, MFSD8, MGAT2, MGME1, MLC1, MLPH, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MMUT, MOCS1, MOCS2, MOGS, MPDU1, MPI, MPV17, MRPL44, MRPS22, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-RNR1, MT-RNR2, 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, MT-TP, MT-TQ, MT-TR, MT-TS1, MT-TS2, MT-TT, MT-TV, MT-TW, MT-TY, MTFMT, MTHFR, MTPAP, MTR, MTRFR, MTRR, MYO5A, MYOT, NAGA, NAGLU, NAGS, NARS2, NAXD, NAXE, NBAS, NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA2, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF4, NDUFAF5, NDUFAF6, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NEU1, NEUROD1, NEUROG3, NFE2L2, NFU1, NGLY1, NHLRC1, NIPA1, NKX2-2, NKX6-2, NOTCH3, NPC1, NPC2, NPR2, NRAS, NT5C2, NUBPL, OAT, OCLN, OCRL, OPA3, OSGEP, OTC, OXCT1, PAH, PANK2, PAX4, PC, PCCA, PCCB, PCK1, PCSK9, PCYT2, PDHA1, PDHB, PDHX, PDP1, PDSS1, PDSS2, PDX1, PEPD, PET100, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PFKM, PGAM2, PGAP1, PGK1, PGM1, PHKA1, PHKA2, PHKB, PHKG2, 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