Alg11-cdg

Table of contents:

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

Description

ALG11-CDG is a form of congenital disorders of N-linked glycosylation characterized by facial dysmorphism (microcephaly, high forehead, low posterior hairline, strabismus), hypotonia, failure to thrive, intractable seizures, developmental delay, persistent vomiting and gastric bleeding. Additional features that may be observed include fat pads anomalies, inverted nipples, and body temperature oscillation. The disease is caused by mutations in the gene ALG11 (13q14.3).

Genes related to Alg11-cdg

ALG11

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Alg11-cdg

Intellectual disability
Seizures
Global developmental delay
Generalized hypotonia
Hearing impairment
Microcephaly
Scoliosis
Strabismus
Sensorineural hearing impairment
Muscular hypotonia

And another 14 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.)
— No data available about the known clinical features onset.

Alternative names

Alg11-cdg Is also known as cdg-ip, congenital disorder of glycosylation type 1p, congenital disorder of glycosylation type ip, cdg syndrome type ip, carbohydrate deficient glycoprotein syndrome type ip, cdg1p.

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.

Alg11-cdg Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Congenital Disorders of Glycosylation. By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). SLC35A1, COG5, ALG9, ALG1, ATP6V0A2, COG4, COG6, COG7, COG8, ALG12, SLC35C1, ALG3, ALG6, ALG2, ALG8, DOLK, GNE, MOGS, SRD5A3, DDOST , (...) View the complete list with 14 more genes Panel complete gene list SLC35A1, COG5, ALG9, ALG1, ATP6V0A2, COG4, COG6, COG7, COG8, ALG12, SLC35C1, ALG3, ALG6, ALG2, ALG8, DOLK, GNE, MOGS, SRD5A3, DDOST, DPAGT1, DPM1, DPM3, RFT1, TUSC3, TMEM165, ALG13, ALG11, COG1, MGAT2, MPDU1, MPI, PMM2, B4GALT1 Specificity 3 % Genes 100 %
Congenital disorders of glycosylation (NGS panel for 39 genes). By CGC Genetics (Portugal). SLC35A1, SLC35A2, SSR4, COG5, ALG9, NGLY1, ALG1, COG4, COG6, COG7, COG8, ALG12, SLC35C1, ALG3, ALG6, ALG2, ALG8, DOLK, MOGS, SRD5A3 , (...) View the complete list with 19 more genes Panel complete gene list SLC35A1, SLC35A2, SSR4, COG5, ALG9, NGLY1, ALG1, COG4, COG6, COG7, COG8, ALG12, SLC35C1, ALG3, ALG6, ALG2, ALG8, DOLK, MOGS, SRD5A3, DDOST, DPAGT1, DPM1, DPM2, DPM3, RFT1, STT3B, TMEM165, ALG13, ALG11, STT3A, COG1, MAN1B1, MGAT2, MPDU1, MPI, PGM1, PMM2, B4GALT1 Specificity 3 % Genes 100 %
Congenital disorder of glycosylation type 1P (sequence analysis of ALG11 gene). By CGC Genetics (Portugal). ALG11 Specificity 100 % Genes 100 %
Congenital Disorders of Glycosylation Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SLC35A1, SLC35A2, SSR4, COG5, ALG9, NGLY1, TMEM199, ALG1, ATP6V0A2, COG4, COG6, COG7, COG8, ALG12, SLC35C1, DHDDS, SLC39A8, GMPPA, ALG3, ALG6 , (...) View the complete list with 30 more genes Panel complete gene list SLC35A1, SLC35A2, SSR4, COG5, ALG9, NGLY1, TMEM199, ALG1, ATP6V0A2, COG4, COG6, COG7, COG8, ALG12, SLC35C1, DHDDS, SLC39A8, GMPPA, ALG3, ALG6, ALG2, ALG8, DOLK, GNE, MOGS, SRD5A3, DDOST, CCDC115, MAGT1, DPAGT1, DPM1, DPM2, DPM3, RFT1, TUSC3, STT3B, TMEM165, ALG13, ALG11, STT3A, COG1, COG2, MAN1B1, MGAT2, MPDU1, MPI, ATP6AP1, PGM1, PMM2, B4GALT1 Specificity 2 % Genes 100 %
Mental retardation - different panels. 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 Panel complete gene list RGS7, RIT1, RMRP, BCS1L, RPL10, RPS6KA3, RRAS, SALL1, SC5D, ATXN10, BLM, SCN1A, SCN2A, SCN8A, SCO2, AIMP1, SDCCAG8, SDHA, SDHB, SGSH, SHH, ST3GAL3, ST3GAL5, STIL, SIX3, SKI, SLC12A6, SLC16A2, SLC17A5, SLC1A4, BRAF, SLC25A1, SLC25A15, SLC25A16, SLC2A1, SLC31A1, SLC35A1, SLC35A2, SLC35A3, SLC4A4, SLC6A1, SLC6A3, SLC6A8, SLC9A6, SMARCA2, SMARCA4, SMARCB1, SMARCE1, ARID1A, SMC1A, KDM5C, SMPD1, SMS, SNAP29, SIK1, SOS1, SOS2, SOX10, SOX2, SOX3, SOX5, SPG11, SPTAN1, SSR4, STIM1, PLK4, CDKL5, STXBP1, SUOX, SURF1, BUB1B, SYN1, SYNGAP1, SYP, TAF1, TAF2, TAT, TBCE, TBR1, TCF12, TCF20, TCF4, TGFBR1, TGFBR2, TGIF1, TH, THRB, ACO2, TIMM8A, NKX2-1, TSPAN7, ACOX1, MED12, TPI1, TREX1, TRIO, TRIP12, TSC1, TSC2, CEP41, TUBA8, TUBB2A, TUBG1, UBE2A, UBE3A, USP9X, KDM6A, VLDLR, VRK1, WNT1, WWOX, XPA, ZIC2, RNF113A, KAT6A, SCAPER, ZNF711, ZNF81, ACTB, ARL6, FTSJ1, HDAC8, KIF4A, MCOLN1, NSDHL, RLIM, UBE3B, USP27X, ZBTB20, ERLIN2, FBXL4, CTCF, CA2, CA5A, SLC12A5, CA8, CNTNAP2, CACNA1C, CACNA1G, CACNA2D2, HDAC4, FMN2, CCDC78, NSD1, CAD, RAB18, AUTS2, PCDH19, NLGN4X, NLGN3, SHANK3, SHANK2, SCYL1, ACTG1, ELOVL4, TMEM237, MRPS22, ARHGEF9, DEAF1, CAPN10, COG5, ZEB2, PIGT, PPP1R15B, CASK, SNX14, CASP2, MICU1, CBL, SHOC2, MBTPS2, GPHN, ANKH, CBS, PUS1, JAM3, SETBP1, ALG9, LRPPRC, GEMIN4, ADNP, CCNA2, BSCL2, KMT2B, ARFGEF2, PANK2, NDUFAF5, PLCB1, SAMHD1, APTX, MPLKIP, PCNT, SFXN4, TBC1D20, MGME1, DNAJC5, UPB1, TRIM32, NLRP3, RAB39B, FBXO31, TUBGCP4, BCAP31, ZNF423, UBR1, COQ8A, FIG4, HAX1, STAMBP, ZMYND11, SRCAP, CLP1, RAB3GAP1, EXOSC2, ACVR1, CDON, RAB3GAP2, COLEC11, CENPJ, WAC, BRWD3, GMNN, GJC2, CDH15, KAT6B, NDE1, PORCN, ACY1, CDK5, PDSS1, CDK6, AFF4, PGAP2, EXOSC3, CEP83, FKRP, ARID2, ARID1B, ARX, GPT2, SPATA5, TUBGCP6, PHF6, TMCO1, ELP2, PECR, ALG1, ATP6AP2, ASXL1, PRIMA1, SETD2, DEPDC5, ZDHHC9, ATP6V0A2, SPART, RNASEH2A, IER3IP1, CENPE, SLC39A6, COG4, COG6, COG7, COG8, IFT27, RTTN, PMPCA, CDK5RAP2, ASCC3, NAA10, BBS7, POGZ, KCNT1, MMAA, IFIH1, GBA2, ASPM, THOC2, NALCN, POMGNT1, CHD2, FRAS1, DOCK7, ALG12, CHKB, COQ4, CNKSR1, CNKSR2, POMT2, ISCA2, SLC25A22, TECPR2, KIAA0586, CCDC88C, AARS, SNX27, TTC8, CHD8, SLC35C1, B3GLCT, CLCN4, SPRED1, NUBPL, CHAMP1, SMOC1, UBR7, FRY, NDUFA11, UPF3B, MBD5, APOPT1, L2HGDH, ZC3H14, CYP2U1, CHD7, CLIC2, PHF8, TPP1, CLN3, CLN5, ZFYVE26, TUBA1A, CLN6, TUBB4A, CLN8, BCOR, HACE1, SERAC1, FARS2, TBC1D7, RNF125, GTF2H5, RMND1, ANKRD11, DYM, PDHX, ABHD5, INPP5E, ACAD9, AHI1, SATB2, RNASET2, BRAT1, VPS13B, RBM28, COL18A1, KCTD7, COL4A1, COL4A2, COL4A3BP, ADAR, COX10, COX15, GMPPA, GMPPB, MED13L, PEX26, PDSS2, ALG3, SLC13A5, ALG6, ALG2, ALG8, PNPT1, PIGO, ETHE1, ACBD6, CRADD, DOLK, KIF1BP, CREBBP, DHTKD1, PGAP3, MED23, MED17, NDUFA12, APC2, RNASEH2C, PTRH2, POC1A, WDR62, TCTN3, MMACHC, NECAP1, KANSL1, FAM126A, SIL1, EHMT1, FTO, SMC3, RABL6, MFF, MOGS, CEP104, LARP7, VPS37A, ZC4H2, CTDP1, TMEM216, WDR45B, PRMT9, CTNNB1, ADAT3, MMADHC, COQ2, AHDC1, ZCCHC8, CTSD, CTSF, DDX59, KATNAL2, RAB40AL, ARL13B, TANGO2, FRMD4A, ANO10, CCDC88A, DARS2, CUL4B, PRMT7, SETD5, TTC21B, OFD1, RNASEH2B, ADK, PGAP1, LAS1L, TRAPPC11, TCTN2, CPLANE1, SRD5A3, CEP63, MFSD2A, POMGNT2, WDR73, GON4L, TRMT1, PIGG, NSUN2, KRBOX4, PIGV, TCTN1, TMEM135, CSPP1, FAR1, TM4SF20, TTI2, POMK, NARS2, BBS10, HEPACAM, PTCHD1, HGSNAT, UNC80, WDR81, BBS12, DAG1, DARS, C12orf65, CKAP2L, HIKESHI, TMEM138, DBT, METTL23, PARP1, DCX, DDC, ESCO2, DDOST, ACSF3, DDX3X, WDPCP, BBIP1, CCDC28B, CCDC115, ADRA2B, D2HGDH, TMEM67, TRMT10A, MFSD8, DHCR24, B3GALNT2, DHCR7, DHFR, CYB5R3, DIAPH1, MED25, NIPBL, MAGT1, DKC1, CCDC22, WDR45, EMC1, DLD, WASHC5, FRMPD4, SETD1A, KDM6B, DLG3, CEP290, SZT2, ZBTB40, IQSEC2, KIAA0556, KDM1A, CEP135, ADSL, DDHD2, RPGRIP1L, TBC1D24, SHROOM4, CC2D2A, SOBP, DMD, DIP2B, CEP152, ZSWIM6, DMPK, EPG5, KLHL15, ASXL3, ZNF526, EARS2, RSPRY1, CCBE1, NEXMIF, ROGDI, C12orf57, TBL1XR1, DYNC1H1, DNM1, DNM1L, DNMT3A, DNMT3B, DCPS, DPAGT1, BBS9, DPH1, PACS1, DPM1, DPM2, DPM3, POLR3A, DPP6, DPYD, CRBN, ATP13A2, RFT1, CC2D1A, TUSC3, PYCR2, POLR3B, IFT172, KIF7, PRRT2, DNAJC19, STT3B, STRA6, CLPB, TMEM165, GATAD2B, TUBB2B, TRAPPC9, POC1B, EFTUD2, ALG13, HUWE1, DYRK1A, LINS1, SLC6A17, AGA, EEF1A2, EEF1B2, MEGF8, ALG11, AGPAT2, EIF2AK3, EIF2S3, EMX2, ENTPD1, EP300, AHCY, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, EZH2, ACSL4, FANCD2, FASN, AK1, FKTN, FGD1, FGFR1, FGFR2, FGFR3, FH, TMEM231, ISPD, FLNA, FMR1, AFF2, FOXG1, FOXP1, AKT3, MTOR, PET100, FUCA1, ALDH3A2, GABRA1, ALDH5A1, GABRB3, GAD1, GALE, B4GALNT1, GALT, GAMT, GATM, GCH1, GCSH, GDI1, GFAP, GK, GLDC, GLI2, GLI3, GNAO1, GNAS, GNPAT, GNS, GPC3, GABBR2, ADGRG1, TECR, GRIA3, GRIK2, GRIN1, GRIN2A, GRIN2B, GRM1, GRN, GSS, GTF2E2, GUSB, AMT, HIST3H3, HIST1H4B, HSD17B10, HCCS, HCFC1, HCN1, HERC2, HESX1, ANK3, HLCS, HMGB3, HNRNPK, HOXA1, HPD, HPRT1, HRAS, IDS, IDUA, IGF1, AP1S1, AP1S2, AP3B1, AP4B1, AP4E1, AP4M1, AP4S1, IKBKG, IL1RAPL1, ABCC9, IMPA1, INPP4A, ABCD1, STT3A, ITPA, KATNB1, KCNA2, KCNB1, KCNH1, KCNJ11, KCNJ6, KCNK9, KCNQ2, KCNQ3, KIF2A, KIF5C, KIF11, KPTN, KRAS, L1CAM, LAMA1, LAMA2, LAMB1, LAMC3, LAMP2, LARGE1, COG1, LIG4, LRP2, LZTFL1, LZTR1, MAB21L2, SMAD4, MAF, MAG, ABCD4, MAGEL2, MAN1B1, MAN2B1, MANBA, MAOA, MAP2K1, MAP2K2, ARHGEF6, MASP1, MAT1A, MCCC1, MCCC2, MCPH1, MECP2, MEF2C, MEIS2, MGAT2, MID1, MID2, MKKS, MKS1, KMT2D, MLYCD, MOCS1, MOCS2, MPDU1, MPDZ, MPI, ASAH1, MT-CO1, MT-CO2, MT-CO3, ASL, MT-ND5, MTR, MTRR, MT-TK, MT-TL1, MT-TS1, MT-TV, MMUT, ASNS, MVK, MYCN, ASPA, MYO5A, MYT1L, NAGA, NAGLU, NBN, NDP, NDST1, NDUFA1, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS7, NDUFS8, NDUFV1, NEU1, NF1, NFIX, NHS, PNP, NPHP1, NR2F1, NRAS, ATP1A2, NRXN1, ATP1A3, NT5C2, NTRK1, OCLN, OCRL, ATP2A2, OPHN1, ORC1, OTX2, ATP6V1B2, PAFAH1B1, PAK3, PAX6, PC, ATP7A, AIFM1, PDE4D, PDE6D, PDHA1, ATR, PEPD, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX6, ATRX, PEX7, KIF1A, PGK1, AUH, PGM1, PGM3, PHGDH, PIGA, PIGN, PIK3CA, PIK3R1, PIK3R2, PLP1, PMM2, PNKP, POMT1, B4GALT1, PPOX, B4GALT7, PPP2R1A, PPP2R5D, PPT1, PQBP1, PRKCG, PRKRA, PRODH, PRPS1, PRSS12, SLC33A1, PTCH1, PTDSS1, PTEN, PTPN11, BBS1, BBS2, BBS4, BBS5, PURA, NECTIN1, PEX5, PYCR1, ALDH18A1, QARS, RAB27A, RAD21, RAF1, RAI1, RALGDS, BCKDHA, RARB, BCKDHB, RASA2, KDM5A, RBBP8, RELN Specificity 1 % Genes 100 %
Congenital Disorders of Glycosylation (CDG). By MGZ Medical Genetics Center (Germany). SLC35A1, SLC35A2, SSR4, COG5, ALG9, ALG1, COG4, COG6, COG7, COG8, ALG12, SLC35C1, DHDDS, GMPPA, ALG3, ALG6, ALG8, DOLK, MOGS, SRD5A3 , (...) View the complete list with 18 more genes Panel complete gene list SLC35A1, SLC35A2, SSR4, COG5, ALG9, ALG1, COG4, COG6, COG7, COG8, ALG12, SLC35C1, DHDDS, GMPPA, ALG3, ALG6, ALG8, DOLK, MOGS, SRD5A3, DDOST, DPM1, DPM3, RFT1, TUSC3, STT3B, TMEM165, ALG13, ALG11, STT3A, COG1, MAN1B1, MGAT2, MPDU1, MPI, PGM1, PMM2, B4GALT1 Specificity 3 % Genes 100 %
AllNeuro panel. By Centogene AG - the Rare Disease Company (Germany). BCS1L, ROR2, RPL10, BDNF, RPS6KA3, RTN2, RYR1, SACS, BIN1, SBF1, SCN10A, SCN1A, SCN1B, SCN2A, SCN3A, SCN4A, SCN5A, SCN8A, SCN9A, SCO1 , (...) View the complete list with 1177 more genes Panel complete gene list BCS1L, ROR2, RPL10, BDNF, RPS6KA3, RTN2, RYR1, SACS, BIN1, SBF1, SCN10A, SCN1A, SCN1B, SCN2A, SCN3A, SCN4A, SCN5A, SCN8A, SCN9A, SCO1, SCO2, SCP2, AIMP1, SDCCAG8, SDHA, SGCA, SGCB, SGCD, SGCE, SGCG, SGSH, SHH, ST3GAL3, ST3GAL5, STIL, SIX3, SIX6, SKI, DST, SLC12A6, SLC16A2, SLC17A5, SLC1A3, SLC20A2, SLC22A5, BRAF, SLC25A12, SLC25A3, SLC25A4, SLC2A1, SLC35A1, SLC35A2, SLC3A1, SLC4A4, SLC6A1, SLC6A3, SLC6A5, SLC6A8, SLC9A6, SMARCA2, SMARCA4, SMARCB1, ARID1A, SMC1A, KDM5C, SMN1, SMN2, SMPD1, SMS, SNAP29, SNCA, SNCAIP, SNCB, SNX3, SOD1, SORL1, SOS1, SOX10, SOX3, SPG11, ATL1, SPAST, SPG7, SPR, SPTAN1, SPTBN2, SPTLC1, SPTLC2, CDKL5, STUB1, STXBP1, SUCLA2, SUCLG1, SURF1, SYN1, SYNGAP1, SYNJ1, SYP, TAF1, TAF2, TARDBP, TAZ, TBCE, TBX1, TWNK, TCAP, TCF4, TFAP2A, TFAP2B, TFG, TG, TGFB1, TGFB2, TGFBR1, TGFBR2, TGIF1, TH, ACO2, TIMM8A, NKX2-1, TK2, TLR3, TLR5, TSPAN7, TNF, ACOX1, TNFSF4, TNNT1, MED12, GIGYF2, TPM2, TPM3, TRAF3, TREX1, TRPS1, TSC1, TSC2, TSFM, CEP41, TSHB, MYOT, TTN, TTPA, TTR, TUBA4A, TUBA8, TWIST1, TYROBP, UBA1, UBE2A, UBE3A, UBQLN2, UCHL1, UMPS, UQCRB, USP8, USP9X, KDM6A, VAMP1, VAPB, VAX1, VCP, VDAC1, VEGFA, VHL, VLDLR, BEST1, VRK1, WFS1, WNT3, WNT5A, WNT7A, WWOX, XBP1, XK, YARS, YWHAE, ZIC2, ZIC3, ACTA1, ZBTB16, ACTA2, ZBTB18, ZNF711, ZNF81, CNBP, ACTB, ARL6, FTSJ1, HDAC8, LPIN1, NSDHL, UNC93B1, VPS35, ATP8A2, ERLIN2, FBXO7, AAAS, GFM1, PRX, CA8, WNT10A, CNTNAP2, FOXP2, CACNA1A, CACNA1B, CACNA1C, CACNA1D, CACNA1H, CACNA1S, ANO3, SLC5A7, CACNB4, CACNG2, HDAC4, ARHGEF10, CCDC78, SLC25A20, NSD1, RAB18, CERS1, PCDH19, NLGN4X, NLGN3, SHANK3, SHANK2, HTRA2, IRX5, ACTG1, SLC25A19, ELOVL4, TMEM237, LPIN2, NPC2, WNK1, ARHGEF9, PINK1, AMN, CAPN3, COG5, ZEB2, DNAJB6, ALX1, CASK, CASR, CAV3, CBL, SHOC2, MBTPS2, DNAJC6, DIAPH3, TSEN34, PUS1, VANGL1, CHCHD10, SETBP1, HPS3, ALG9, LDB3, LRPPRC, KRIT1, ADNP, ZNF335, BSCL2, HPS4, ARFGEF2, ABHD12, PANK2, NDUFAF5, NOP56, PLCB1, SAMHD1, GDAP1, TRIM2, TP63, APTX, SELENON, PCNT, LIMS2, CCT5, DNAJC5, TGM6, YAP1, SLC19A3, PNPLA6, NFU1, UPB1, PARK7, TRIM32, NLRP3, EFHC1, RAB39B, BSND, CD36, KIF1B, SCARB2, CD320, BCAP31, MCEE, CIZ1, ZNF423, COQ8A, LITAF, FIG4, MFN2, CD59, CD96, BCKDK, ERLIN1, PRICKLE1, HPS5, EXOSC8, NIPA1, RAB3GAP1, MLC1, SYNE2, SYNE1, TNPO3, CDON, OPTN, RAB3GAP2, TIRAP, CHSY1, BICD2, CPA6, CENPJ, ZFR, RRM2B, CDK11A, WAC, DTNBP1, BRWD3, TPK1, AASS, ADGRV1, GJC2, ACVRL1, CDH15, KAT6B, NDE1, PORCN, ACY1, PDSS1, TREM2, CD207, EXOSC3, REEP2, TRPM7, TRPM6, FKRP, ARID1B, ARX, TRPV4, TUBGCP6, PHF6, TMCO1, RBFOX1, ALG1, ATP6AP2, TMLHE, ASXL1, TICAM1, HPSE2, SETD2, DEPDC5, ZDHHC9, ATP6V0A2, SPART, RNASEH2A, IER3IP1, LRRK2, COG4, COG6, COG7, COG8, IFT27, CDK5RAP2, NAA10, GRIP1, CNTNAP4, CFL2, RIN2, BBS7, ADAM10, POGZ, ATPAF2, CAMTA1, HPS6, NDUFAF1, KCNT1, MMAA, TDP1, MAGI2, GBA2, AANAT, ASPM, VPS13A, CHAT, FGD4, POMGNT1, TTBK2, CHD2, DOCK8, MTO1, KANK1, MMAB, KIF21A, ALG12, KCNK18, CHRM3, CHRNA1, CHRNA2, CHRNA4, CHRNB1, CHRNB2, CHRND, CHRNE, CHRNG, DDHD1, POMT2, CISH, SLC25A22, TECPR2, CCDC88C, AARS, TTC8, FLVCR2, GPR143, CHD8, CLCN1, SLC35C1, CLCN2, B3GLCT, CLCNKA, CLCNKB, NUBPL, PRICKLE2, ZDHHC15, VIPAS39, NDUFA11, SPG21, SUMF1, UPF3B, MBD5, CYP2U1, CHD7, CLIC2, SLC9A9, PHF8, TPP1, GNB4, CLN3, CLN5, ZFYVE26, TUBA1A, CLN6, TUBB3, TUBB4A, CLN8, THAP1, BCOR, BLOC1S3, AARS2, NDUFAF4, RNF135, FA2H, ICK, ELOVL5, ANKRD11, SBF2, ABHD5, RARS2, INPP5E, ACAD9, AHI1, NHLRC1, RNASET2, BRAT1, CCM2, CNTN1, LHX4, VPS13B, AGK, COL12A1, COL18A1, KCTD7, COL4A1, COL4A2, COL6A1, COL6A2, COL6A3, COL7A1, AP5Z1, COLQ, ADAR, COX10, COX15, COX6A1, COX6B1, GMPPB, NLRP12, CP, PEX26, ABAT, LMBRD1, PDSS2, ALG3, SLC13A5, SYT14, ALG6, ALG2, ALG8, KIRREL3, MYH14, PIGO, ETHE1, CPT2, CR1, FREM1, CRADD, DOLK, CREBBP, DHTKD1, ADCY5, GNE, MED23, PTF1A, MED17, INF2, CRYAB, NDUFA12, KNL1, RNASEH2C, B9D1, CISD2, TACO1, CSF1R, CSF2RB, BOLA3, PLEKHG4, WDR62, TCTN3, MMACHC, CHMP2B, FAM126A, SIL1, EHMT1, EXOC8, FTO, SMC3, FLVCR1, CST3, CSTB, MOGS, VPS37A, CTDP1, TMEM216, MARS2, LRSAM1, CTNNB1, MMADHC, COQ2, CTSD, COQ9, SLC30A10, RNF170, TMEM126A, RAB40AL, ARL13B, C19orf12, ANO10, MTPAP, DARS2, CUL4B, CWF19L1, TTC21B, OFD1, RNASEH2B, MAMLD1, ADK, PGAP1, NHEJ1, TRAPPC11, TCTN2, DCAF17, REEP1, CPLANE1, SRD5A3, CEP63, POMGNT2, CYP11B2, RETREG1, NSUN2, TTC19, PIGV, CYP27A1, TMEM70, TCTN1, CTC1, MTMR14, CSPP1, TTI2, POMK, PIEZO2, BBS10, HEPACAM, CYP7B1, HGSNAT, ZFYVE27, DOK7, WDR81, BBS12, DAG1, NAT8L, C12orf65, FOXRED1, TMEM138, DBT, RBFOX3, DCTN1, DCX, ESCO2, ZCCHC12, DDOST, ACSF3, ANO5, TSEN54, DES, WDPCP, NDUFAF2, BBIP1, CCDC28B, C9orf72, TMEM67, TSEN2, MFSD8, DGUOK, DHCR7, NDUFAF6, B9D2, DHH, FBXO38, MED25, NIPBL, MAGT1, DKC1, WDR45, DLD, WASHC5, ZNF592, RUBCN, DLG3, CEP290, SZT2, IQSEC2, IFT140, CEP135, SMCHD1, ADSL, PLEKHG5, DDHD2, FASTKD2, RPGRIP1L, TBC1D24, SHROOM4, ARHGAP31, CC2D2A, SOBP, DMD, CEP152, ASXL3, EARS2, SH3TC2, NEXMIF, ROGDI, C12orf57, TBL1XR1, DNAH9, UQCRQ, DYNC1H1, DYNC2H1, MTFMT, DNM1L, DNM2, DNMT1, NDUFAF3, COASY, DPAGT1, BBS9, PIK3R5, DPM1, DPM3, POLR3A, HSPB8, STRADA, CRBN, ATP13A2, RFT1, PREPL, DRD2, CC2D1A, DRD3, TUSC3, PNPO, POLR3B, DSC3, KIF7, PRRT2, DNAJC19, SNIP1, SEPSECS, SRPX2, TMEM165, PNPLA2, TUBB2B, TRAPPC9, EFTUD2, ALG13, HUWE1, DYRK1A, WDR48, LINS1, DYSF, TOR1A, EBP, TYMP, AFG3L2, EDN3, AGA, EDNRB, AGL, EEF2, EGR2, ALG11, ARSI, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF4E, AGRN, EIF4G1, ELK1, EMD, EMX2, ENO3, ENTPD1, EOMES, EP300, EPB41L1, COA5, SDHAF1, RNU4ATAC, AGXT, EPM2A, AHCY, ERBB4, ERCC1, ERCC2, ERCC5, ERCC6, ETFA, ETFB, ETFDH, F2, F5, ACSL4, FADD, FANCB, FBLN5, FCGR2B, FKTN, FGA, FGD1, FGF10, FGF14, FGFR1, FGFR2, FGFR3, FH, FHL1, KBTBD13, TMEM231, ISPD, FLNA, FLNC, FLRT1, FMR1, AFF2, FOLR1, FOXG1, FOXP1, AKT1, AKT3, MTOR, ALAD, FXN, FRG1, FTL, FUS, ALDH3A2, ACKR1, FZD9, ALDH4A1, GAA, GABRA1, ALDH5A1, GABRB3, GABRD, GABRG2, GAD1, GALC, B4GALNT1, GALNS, GAMT, GAN, ALDOA, GARS, ALDOB, GATM, GBA, GBE1, GCDH, GCH1, GCSH, GDI1, GDNF, GFAP, GFER, GFPT1, ALMS1, GJB1, GK, GLB1, GLDC, GLI2, GLI3, GLRA1, GLRB, ALOX5AP, GM2A, GNAL, GNPAT, GNS, ALS2, GOSR2, GP1BA, SETX, GPC3, ALX3, ALX4, AMACR, ADGRG1, TECR, GRIA3, GRID2, GRIK2, GRIN1, GRIN2A, GRIN2B, GRM1, GRN, GSN, AMPD1, AMPD2, GUSB, GYG1, GYS1, AMT, ABCB7, HSD17B10, HADHA, HADHB, ANG, HCCS, HTT, HERC2, HESX1, HEXA, HEXB, HFE, HINT1, HK1, ANK3, HMGCS2, HNRNPDL, HOXA1, HOXD10, HPCA, HPD, HPRT1, HPS1, HRAS, HSD17B4, DNAJB2, HSPB1, HSPB3, HSPD1, HYAL1, NOD2, ICAM1, IDS, IDUA, IFRD1, IGBP1, IGF1, IGHMBP2, AP1S1, AP1S2, AP3B1, ABCC6, AP4B1, AP4E1, AP4M1, AP4S1, ABCC8, ELP1, IKBKG, IL11RA, IL1RAPL1, IL1RN, INS, ABCD1, FOXP3, APOE, ITM2B, ITPR1, JRK, APP, KARS, KCNA1, KCNC3, KCND3, KCNE5, KCNJ1, KCNJ10, KCNJ11, KCNK9, KCNMA1, KCNQ2, KCNQ3, KIF1C, KIF5A, KLF8, KIF11, KRAS, AR, KRT5, L1CAM, LAMA2, LAMB1, LAMB2, LAMC3, LAMP2, LARGE1, LBR, LDHA, COG1, LGI1, ARG1, LMNA, LMNB1, LRP2, LYZ, LZTFL1, MAG, ABCD4, MAGEL2, MAN1B1, MAOA, ARHGEF6, MAPK10, MAPT, MARS, MASP1, MATR3, MCPH1, MECP2, MEF2C, A2M, MET, MGAT2, MID1, ATXN3, MKKS, MKS1, ARSA, KMT2D, ARSB, ARSE, MPDU1, MPDZ, MPI, MPV17, MPZ, MRE11, ASAH1, ASCL1, MSX1, MSX2, MTHFR, MTM1, MTMR2, ASL, MTR, MTRR, MUSK, MMUT, ASNS, MVK, MYCN, ASPA, MYF6, MYH7, MYH9, ASS1, MYO5A, NAGA, NAGLU, NBN, NDP, NDRG1, NDST1, NDUFA1, NDUFA10, NDUFA2, NDUFA4, NDUFA9, NDUFB3, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NEB, NEDD4L, NEFH, NEFL, NEU1, NF1, NFIX, ATCAY, NGF, NHS, NOG, NOL3, NOS2, NOTCH2, NOTCH3, NPC1, NPHP1, NPHP3, ATIC, ATM, NRAS, NRG1, ATP1A2, NRXN1, ATP1A3, NT5C2, NTRK1, NTRK2, NXF5, FRMD7, OCLN, OCRL, ATP2A1, ATP2A2, OPA1, OPA3, OPHN1, SIGMAR1, ATP2B3, ATP2B4, ATP5F1E, ACACA, ORC1, OTC, BLOC1S6, PAFAH1B1, PAH, PAK3, PRKN, PAX6, PC, PCBD1, ATP7A, ATP7B, PCK2, CHMP1A, PDCD10, AIFM1, ALDH7A1, PDE6D, PDE8B, ACADL, PDHA1, PDK3, ATR, PDYN, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX3, PEX6, ATRX, PEX7, PFKM, KIF1A, PFN1, PGAM2, PGK1, ACADM, PGM1, PHKA1, PHYH, SERPINI1, PIGA, PIGL, PIGN, PIK3CA, PIK3R2, ACADS, PLA2G6, PLEC, PLP1, ACADSB, PMM2, PMP22, PRRX1, PHOX2B, PNKD, PNKP, POLG, POLG2, ACADVL, POMT1, B4GALT1, ACAT1, PPT1, PQBP1, PRKAG2, BAG3, PRKCG, PRKCH, PRKRA, PRNP, PROP1, PRPS1, HTRA1, PRSS12, PSAP, SLC33A1, PSEN1, PSEN2, TAS2R38, PTCH1, PTEN, PTPN11, BBS1, BBS2, PTS, BBS4, BBS5, NECTIN1, PEX19, PEX2, PEX5, ALDH18A1, PYGM, QARS, QDPR, RAB7A, RABGGTA, RAD21, RAD50, RAF1, RAI1, RANBP2, BCKDHA, RAPSN, BCKDHB, RBBP8, RBM10, RBM8A, PRPH2, RELN, RET Specificity 1 % Genes 100 %
Congenital Disorders of Glycosylation (CDG) Panel. By CeGaT GmbH (Germany). SLC35A1, SLC35A2, COG5, ALG9, ALG1, COG4, COG6, COG7, COG8, ALG12, SLC35C1, ALG3, ALG6, ALG2, ALG8, DOLK, MOGS, SRD5A3, DDOST, DPAGT1 , (...) View the complete list with 14 more genes Panel complete gene list SLC35A1, SLC35A2, COG5, ALG9, ALG1, COG4, COG6, COG7, COG8, ALG12, SLC35C1, ALG3, ALG6, ALG2, ALG8, DOLK, MOGS, SRD5A3, DDOST, DPAGT1, DPM1, DPM2, DPM3, RFT1, TMEM165, ALG13, ALG11, COG1, MGAT2, MPDU1, MPI, PGM1, PMM2, B4GALT1 Specificity 3 % Genes 100 %

You can get up to 11 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

ORPHANET OMIM Rare Disease Symptoms Checker

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like VERHEIJ SYNDROME; VRJS POROKERATOSIS 2, PALMAR, PLANTAR, AND DISSEMINATED TYPE; POROK2 NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1 NEPHROGENIC DIABETES INSIPIDUS