Annotation Detail
Information
- Associated Genes
- PARP4 ALOX5AP ATP12A ATP4B ATP7B BRCA2 KLF5 CDK8 CDX2 RCBTB2 CLN5 COL4A1 COL4A2 CPB2 DACH1 DCT GPR183 EDNRB EFNB2 ELF1 ERCC5 ESD F7 F10 FGF9 FGF14 GPC5 FOXO1 FLT1 FLT3 GAS6 GJA3 GJB2 GPR12 GPR18 MLNR GTF2F2 GTF3A HMGB1 HTR2A ING1 PDX1 KPNA3 IPO5 LAMP1 LCP1 LIG4 LMO7 MAB21L1 SMAD9 MIPEP NEK3 PABPC3 PCCA PCDH8 PCDH9 UBL3 POU4F1 DNAJC3 RAP2A RB1 RFC3 RFXAP RNF6 RPL21 ATXN8OS SGCG SLC7A1 SLC10A2 SLC15A1 SOX1 TFDP1 TPP2 TPT1 TRPC4 TUBA3C UCHL3 ZIC2 ZMYM2 IFT88 STK24 CUL4A TNFSF11 IRS2 SCEL SUCLA2 DLEU2 TSC22D1 PROZ ARHGEF7 CDC16 CCNA1 CLDN10 MTMR6 DCLK1 ZMYM5 ITGBL1 KL TM9SF2 ITM2B MTRF1 UTP14C NUP58 TBC1D4 GPC6 FRY MBNL2 FARP1 LPAR6 SLC25A15 LHFPL6 TRIM13 USPL1 MRPS31 SPRY2 ABCC4 SAP18 DLEU1 TUBGCP3 N4BP2L2 PIBF1 OLFM4 POSTN TNFSF13B GJB6 HSPH1 WASF3 SUGT1 CNMD SOX21 WBP4 AKAP11 KLF12 EXOSC8 RASA3 FNDC3A DZIP1 DIS3 MYO16 PDS5B MYCBP2 VWA8 ZC3H13 SPART LRCH1 ATP11A MCF2L MTUS2 DOCK9 TGDS SLITRK5 FBXL3 SACS INTS6 LATS2 CKAP2 NUFIP1 NBEA OXGR1 PCDH17 RGCC MED4 DNAJC15 ALG5 VPS36 POLR1D CRYL1 PHF11 POMP UFM1 ATP8A2 IL17D NDFIP2 MPHOSPH8 BIVM SOHLH2 TMCO3 ENOX1 ARGLU1 DCUN1D2 RCBTB1 PSPC1 NUDT15 GPALPP1 TNFRSF19 SUPT20H ANKRD10 RAB20 NAXD UGGT2 PCID2 CENPJ THSD1 RNF17 CYSLTR2 SPRYD7 COG6 KLHL1 RBM26 XPO4 PCDH20 UPF3A MRPL57 SMIM2 POGLUT2 CARS2 OBI1 NAA16 RNASEH2B DHRS12 GRTP1 BORA RUBCNL PROSER1 TDRD3 CDADC1 CAB39L DIAPH3 CCDC70 COG3 SETDB2 KATNAL1 KBTBD7 SLITRK6 EBPL TMTC4 MEDAG ABHD13 ZIC5 GGACT KBTBD6 STARD13 N4BP2L1 TEX30 TPTE2 EPSTI1 ADPRHL1 SLITRK1 KCTD12 ARL11 WDFY2 TEX29 CSNK1A1L RXFP2 TEX26 SLAIN1 PRR20A SPACA7 RNF113B FAM216B LACC1 HNRNPA1L2 B3GLCT DGKH CCDC122 GPR180 STOML3 COMMD6 CLYBL METTL21C AMER2 USP12 MTIF3 GSX1 ERICH6B CBY2 DLEU7 FAM124A LRRC63 EEF1AKMT1 SKA3 MICU2 SPATA13 LNX2 SLC25A30 ZDHHC20 PAN3 NALCN HS6ST3 DAOA DAOA-AS1 LINC00567 CHAMP1 SIAH3 KCNRG SLC46A3 UBAC2 C1QTNF9 FREM2 NEK5 TMEM255B KCTD4 RASL11A C1QTNF9B SHISA2 NHLRC3 SERP2 SERTM1 ATP11AUN MIR15A MIR16-1 MIR17 MIR18A MIR19A MIR19B1 MIR20A MIR92A1 MIR17HG ALG11 MZT1 PCOTH MIR4500HG CCDC168 URAD ZAR1L SERPINE3 NALF1 CCDC169 PRR20B PRR20C PRR20D PRR20E LMO7DN ACOD1 LINC00543 LOC100288208 ANKRD10-IT1 LINC00427 LINC00402 CCDC169-SOHLH2 BIVM-ERCC5 LINC00558 SWINGN SLC25A30-AS1
- Associated Variants
- GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3
- Source Database
- ClinVar
- Description
- GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3 AND See cases
- ClinVar Allele ID
- 1036685
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-03-10
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001353184
- Observed Origin Sample
- unknown
Drugs