Copyright
©The Author(s) 2024.
World J Clin Cases. Mar 16, 2024; 12(8): 1517-1522
Published online Mar 16, 2024. doi: 10.12998/wjcc.v12.i8.1517
Published online Mar 16, 2024. doi: 10.12998/wjcc.v12.i8.1517
Chromosomal | Genes |
4p16.3 | ZNF141, PDE6B, MYL5, CPLX1, GAK, DGKQ, IDUA, FGFRL1, RNF212, SPON2, CTBP1, MAEA, SLBP, TACC3, FGFR3, LETM1, WHSC1, WHSC2, POLN, RNF4, TNIP2, SH3BP2, ADD1, NOP14, HTT, HGFAC, DOK7, LRPAP1, ADRA2C, ZNF595, ZNF718, ZNF876P, ZNF732, ABCA11P, ZNF721, PIGG, ATP5I, MFSD7, PCGF3, LOC100129917, TMEM175, SLC26A1, TMED11P, LOC100130872, C4orf42, KIAA1530, CRIPAK, FAM53A, TMEM129, SCARNA22, MIR943, C4orf48, NAT8L, HAUS3, MXD4, ZFYVE28, LOC402160, FAM193A, MFSD10, C4orf10, GRK4, C4orf44, RGS12, LOC100133461 |
11p15.5p15.4 | ODF3, SIRT3, IFITM2, IFITM1, IFITM3, PKP3, SIGIRR, PTDSS2, HRAS, MIR210, SCT, DRD4, TALDO1, SLC25A22, PNPLA2, CD151, POLR2L, TSPAN4, AP2A2, MUC6, MUC2, MUC5B, TOLLIP, DUSP8, KRTAP5-1, CTSD, TNNI2, LSP1, TNNT3, MRPL23, H19, IGF2, INS, TH, ASCL2, C11orf21, TSPAN32, CD81, TSSC4, TRPM5, KCNQ1, KCNQ1DN, CDKN1C, PHLDA2, NAP1L4, CARS, OSBPL5, MRGPRG, MRGPRE, ZNF195, BET1L, RIC8A, PSMD13, NLRP6, ATHL1, IFITM5, B4GALNT4, ANO9, RNH1, LRRC56, C11orf35, RASSF7, LOC143666, PHRF1, IRF7, CDHR5, DEAF1, TMEM80, EPS8L2, PDDC1, CEND1, LRDD, RPLP2, SNORA52, EFCAB4A, CHID1, LOC255512, BRSK2, MOB2, LOC338651, KRTAP5-2, KRTAP5-3, KRTAP5-4, KRTAP5-5, FAM99A, FAM99B, KRTAP5-6, LOC402778, SYT8, MIR4298, LOC100133545, MIR675, INS-IGF2, MIR483, IGF2AS, KCNQ1OT1, SLC22A18AS, SLC22A18, SNORA54, C11orf36 |
- Citation: Kaya I. Detection of 4p16.3 deletion and 11p15.5p15.4 gain in a boy by comparative genomic hybridization array: A case report. World J Clin Cases 2024; 12(8): 1517-1522
- URL: https://www.wjgnet.com/2307-8960/full/v12/i8/1517.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v12.i8.1517