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. 2010 Sep 28;103(8):1192–1200. doi: 10.1038/sj.bjc.6605900

Table 2. Recurrent losses observed in the primary tumour and maintained through passages of the xenograft.

Cytogenetic region Start position* End position* Candidate genes
1p34.3 34.4 34.9 MIRN552
2q22.2 141.5 142.1 Not known
4p16.1–15.33 8.5 12.3 GPR78, CPZ, DUB4, DEFB131, DRD5, SLC2A9, MIST, MIRN572, HS3ST1
4p15.2 25.1 26.5 SLC34A2, RBPJ, CCKAR, TBC1D19, STIM2
4q35.1 186.8 189.0 SORB2, TLR3, CYP4V2, KLKB1, F11, MTNR1A, MRPS36P2
7p22.2–7p22.1 3.1 5.9 SDK1, FOXK1, RADIL, PAPOLB, MMD2, RBAK, WIPI2, SLC29A4, FBXL18, MIRN589, ACTB, EGID-654231
7p15.3 20.2 22.6 ITGB8, ABCB5, SP8, SP4, DNAH11, CDCA7L, RAPGEF5, MGC87042
7p15.1 28.3 29.9 CREB5, CPVL, CHN2, PRR15, WIPF3
  30.1 31.1 MIRN550-1, NOD1, GARS, CRHR2, INMT, AQP1, GHRHR, ADCYAP1R1
7p14.3–14.1 32.5 43.0 MIRN550-2, KBTBD2, FKBP9, NT5C3, RP9, BBS9, BMPER, AAA1, NPSR1, TBX20, MERPUD2, hCG1642425, SEPT7, ANLN, AOAH, ELM01, GPR141, TXNDC3, SFRP4, STARD3NL, T cell receptor gamma variable genes, AMPH, RALA, CDC2L5, INHBA, GLI3, TCP1L1, PSMA2, MRPL32
7p12.3 46.0 47.1 EPS15L2
8p21.2 22.9 24.0 TNFRSF10C, TNFRSF10D, TNFRSF10A, CHMP7, R3HCC1, LOXL2, ENTPD4, SLC25A37, NKX3.1, NKX2.6, STC1
  25.2 25.5 GNRH1, KCT9, CDCA2
  25.7 26.3 EBF2, PPP2R2A, SDAD1P1
8p21.1 27.4 28.6 GULOP, CLU, SCARA3, CCDC25, PBK, PNOC, FBXO16, EXTL3
  28.8 30.0 KIF13B, DUSP4, MAP2K1P1
  31.9 32.1 NRG1
9p21.3 20.3 24.7 MIRN491, PTPLAD2, IFNB1, IFNW1, IFNxxx…, LEIF-M, MIRN31, MTAP, CDKN2A, CDKN2B, DMRTA1, ELAVL2
9p21.2–21.1 27.3 28.9 IFNK, LING02
10q22.1 72.1 74.2 SGPL1, PCBD1, SLC29A3, CDH23, PSAP, CHST3, SPOCK2, ASCC1, SSIT4, DNAJB12, CBARA1
10q23.31 89.7 91.4 LIPJ, LIPF, LIPK, LIPN, LIPM, ANKRD22, STAMBPL1, ACTA2, FAS, CH25H, IFIT2, LIPA
10q23.33–24.1 96.5 98.6 CYP2C19, CYP2C9, CYP2C8, PDLIM1, SORBS1, ALDH18A1, TCTN3, ENTPD1, CC2D2B, CCNJ, BLNK, DNTT, TMEM10, TLL2, TM9SF3, PIK3AP1, MIRN606
11q25 131.7 133.7 OPCML, SPATA19, IGSF9B, JAM, PTP4AP2, NCAPD3, THYN1, ACAD8, GLB1L3
17p11.2 19.9 21.6 SPECC1, COTL1P2, MEIS3P2, RNASEH1P1, HSP22, DHRS7B, TMEM11, MAP2K3, KCNJ12
18q21.2–21.33 46.9 61.0 DCC, MBD2, POLI, STARD6, C18orf54, C18orf26, RAB27B, CCDC68, TCF4, AC009271.7, TXNL1, WDR7, AC100775.3, ST8SIA3, ONECUT2, FECH, NARS, ATP8B1, AC022724.8, AC090324.7, NEDD4L, ALPK2, AC104971.5, MALT1, AC104971.5, ZNF532, SEC11L3, GRP, RAX, CPLX4, LMAN1, CCBE1, PMAIP1, AC090377.15, MC4R, AC010928.7, CDH20, RNF152, PIGN, KIAA1468, TNFRSF11A, ZCCHC2, PHLPP, AC015989.11, BCL2, FVT1, VPS4B, SERPINB5, AC036176.8, SERPINB12, SERPINB13, SERPINB4, SERPINB3, SERPINB11, SERPINB7, SERPINB2, SERPINB10, SERPINB8
18q22.3 66.9 68.6 CBLN2
  68.8 72.8 FBXO15, CYB5A, FAUP1, CNDP2, CNDP1
*

UCSC Genome Browser on Human May Assembly; positions are given in megabased.