SNPMiner Trials by Shray Alag

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SNPMiner SNPMiner Trials (Home Page)


Report for Mutation A2215D

Developed by Shray Alag, 2020-2021.
SNP Clinical Trial Gene

There is one clinical trial.

Clinical Trials


1 Congenital Hypothyroidism Due to Thyroglobulin Mutations in an Inbred Brazilian Family: A Novel Compound Heterozygous Constellation and Intronic Mutation Related to Fetal Goiter.

The aim of this study was to identify mutations in the thyroglobulin gene that might be present in patients with fetal goiter and congenital goiter hypothyroidism.

NCT00493103
Conditions
  1. Congenital Hypothyroidism
MeSH:Congenital Hypothyroidism Hypothyroidism
HPO:Congenital hypothyroidism Hypothyroidism

Congenital Hypothyroidism Congenital Hypothyroidism Hypothyroidism Congenital goitrous hypothyroid is commonly linked to thyroglobulin (TG) gene mutations.We aim to identify mutations in the TG gene that might be present in patients with fetal goiter and congenital goiter hypothyroidism.Four related patients with congenital goiter hypothyroidism from an inbred family were studied.Recombinant human TSH stimulation test, DNA sequencing and protein computer analysis were performed.We identified a novel compound heterozygous constellation (IVS30+1G>T/A2215D) in two siblings. --- A2215D ---

The recent described mutation A2215D is located in the ACHE-like domain, which functions as a dimerization domain, facilitating efficient intracellular transport of the protein. --- A2215D ---

Protein computer analysis suggested that the A2215D mutation causes TG structural alterations.A novel compound heterozygous constellation (IVS30+1G>T/A2215D) and the previously described mutation (IVS30+1G>T) that cause severe congenital hypothyroidism due to defective TG synthesis have been identified. --- A2215D ---

Protein computer analysis suggested that the A2215D mutation causes TG structural alterations.A novel compound heterozygous constellation (IVS30+1G>T/A2215D) and the previously described mutation (IVS30+1G>T) that cause severe congenital hypothyroidism due to defective TG synthesis have been identified. --- A2215D --- --- A2215D ---



HPO Nodes


HP:0000821: Hypothyroidism
Genes 438
TGIF1 KMT2D UBR1 SLC16A2 MAGEL2 NODAL ND6 PIEZO1 TBL1X TREX1 NODAL MAGEL2 GTF2IRD1 INSR BRAF DUOXA2 SHH FGFR1 TSHR GNAS ARVCF SHH CTNNB1 YY1 PIK3C2A RREB1 TF SOX3 OCA2 GATA1 NKX2-5 SVBP NDN NKX2-1 GPC1 DLL1 BUB1B FGF8 GAS1 B3GLCT SIM1 FOXH1 CLIP2 BMP4 ELN TPO HIRA DNAH1 GP1BB SLC26A4 FDX2 BAP1 COX1 DLL1 SEC24C TXNRD2 SIX3 NKX2-5 ELN TRH GLIS3 DUOXA2 FOXH1 FOXP3 ADAMTSL1 KATNIP CDON AKT1 TSC1 IGSF1 MEN1 TRMT10A XRCC4 HESX1 PTRH2 GAS1 PDE4D PROP1 TRNW MRAP SUFU TRNL1 TTC37 DACT1 LIG4 PLAGL1 TDGF1 CDON LHX4 GNE IGF2 HPD TMEM67 SHH DISP1 IL7R DUOX2 NKX2-1 PPP1R15B ZIC2 ARL6IP6 THRA DISP1 SRY HSD17B3 SLC25A4 IL2RA ENPP1 FOXH1 TDGF1 AIP EXOSC2 TG LIG4 MDM4 TRNS1 GLI2 POU1F1 FGF8 TRNH LHX4 RAG1 PAX8 DUOX2 PCSK1 SNRPN FMR1 FANCI TREX1 SCN4A FGFR1 PROP1 STAR DCAF17 IFIH1 IYD DNM1L PDE4D EXT2 IRS4 ROBO1 GNAS WDR11 ND1 GATA6 PAX8 ND4 SUFU STAT1 DISP1 RMRP STAG2 BAP1 SIX3 TRNQ RAI1 SNRPN ZBTB20 SMARCB1 LHX4 HSD17B3 NIN ADA RNASEH2B ZIC2 XRCC4 SLC5A5 SKIV2L STAT1 FGF8 SHH HBB OCA2 PIK3CA NODAL FOXP3 CEP57 CEP57 SLC26A4 PTCH1 ZIC2 TRNF ALMS1 KANSL1 FGF8 DLL1 HBB TRHR TRAF7 ACP5 CDON RNASEH2A TRNS2 CDON DUOX2 HNF4A ZFP57 FOXH1 CDON MARS1 CDKN1C TONSL TSHR NNT GAS1 PTEN PTCH1 STUB1 GLI2 ANAPC1 APC TSHB DISP1 BCOR POLG2 IFNG NDN SLC26A4 ANAPC1 FGFR1 CHD7 ACP5 MC2R OCA2 PHF21A ZIC2 FLCN NNT LIFR PLVAP ARNT2 KCNJ10 OTX2 DDOST SMO INSR WFS1 LEP PROKR2 ADAT3 PMM2 FOXI1 RBM28 ITCH APC2 PTRH2 KAT6B NDN RAG2 JAK1 NSD1 SPOP CACNA1C JMJD1C GLI2 BUB1 CDH23 PDGFB TBX1 LEPR TBL2 TBX1 LHX3 FOXE1 FMR1 KAT6B CTNS FOXA2 PPP1R15B FOXP1 RFC2 FUCA1 LEPR RNASEH2C PLAA TRNW LHX3 SGPL1 PROP1 RRM2B LIMK1 HESX1 TWNK WDR4 SMARCE1 SIX3 GLI2 SAA1 FARSA TANGO2 TBC1D24 TRAPPC9 PROP1 TGIF1 SEMA3E CDON TBX1 HNRNPK ALG8 MCM8 FOXI1 IQSEC2 OPA1 HYMAI PRDM16 TRNS1 DEAF1 ZIC2 AFF4 FOXE1 NPHS1 COX2 PAX8 FOXH1 STEAP3 ALX4 NKX2-5 TSC2 COX3 SOX3 FGF8 HBB HESX1 LRP4 RERE POLG MTTP SKI TGIF1 SETBP1 STAT3 SMC1A WFS1 GLI3 GLI2 TDGF1 DCLRE1C ALMS1 POU3F4 HMGA2 PTCH1 LHX4 TERT PIK3CA GLI2 GABRD ITCH GAS1 GAS1 NF2 PTCH1 POU1F1 DYRK1A SLC26A4 SAMHD1 UFD1 C1QBP TGIF1 TREX1 HNF1B ABCC6 PLAG1 GTF2I MAGEL2 TSHR TG SRD5A3 KISS1R KANSL1 PTCH1 EIF2AK3 KCNJ11 CLPB DNAJC19 TDGF1 FUT8 GCH1 GPR161 RAI1 HFE HNRNPK TGIF1 SALL1 SETD2 TSHB SIX3 POMC TDGF1 TRNL2 TRNL1 DLL1 TRNN SNRPN SHH SLC5A5 AKT1 SIX3 DMXL2 TBCK ADAR CHD7 ND5 STAG2 TSHR BUB3 SLC6A17 MAGEL2 TRIP13 MLXIPL HLA-DRB1 AIRE LIG4 PAX8 TPO NKX2-1 APOE NODAL GRM7 ABCC8 LRBA IYD POU1F1 BAZ1B DLL1 COMT DMXL2 TANGO2 FLII IL2RG KCNJ10 NODAL KCNAB2 CTNS PRKAR1A KDM6A SALL1 BTNL2 DISP1
Protein Mutations 2
A2215D T92A
SNP 0