CD34, HTC2, TP53, BAP1, ABL1, CDKN2A, MECOM, CCR7, CSF3, MYC, PTEN, BCR, EGFR, GATA2, DERL1, CD19, ERBB2, FLT3, IGF1R, IKZF1, RUNX1, CD33, CTNNB1, GNAQ, KMT2A, NCAM1, SHOX, TBX1, SETBP1, SAMD9
CD34, HTC2, TP53, BAP1, ABL1, CDKN2A, MECOM, CCR7, CSF3, MYC, PTEN, BCR, EGFR, GATA2, DERL1, CD19, ERBB2, FLT3, IGF1R, IKZF1, RUNX1, CD33, CTNNB1, GNAQ, KMT2A, NCAM1, SHOX, TBX1, SETBP1, SAMD9, ALK, B2M, CSF3R, DGCR, EIF1AX, ESR1, FANCB, FGF1, GNA11, HCCS, HSPB1, HSPB2, IGH, KIT, KRAS, MTTP, NF1, NRAS, PTPN11, RARS1, RB1, SHH, SMARCB1, SRY, STAT3, ELOC, HSPB3, SF3B1, PERP, GOLPH3, ASXL1, SAMD9L, H3P10, ADD1, ANXA7, BIRC5, APP, ATRX, CCND1, BCL6, OPN1SW, FOXL2, BRAF, CAT, CBFB, CBL, CBS, CD14, CD22, CD68, CDKN1A, CEBPA, COL5A1, CSF1R, CSF2RA, NKX2-5, DCC, DFNB20, EGF, EGR1, ELAVL2, EPO, ESD, ETV6, EVPL, EWSR1, FBN2, FGF3, FGFR2, FRA7G, FUT1, GATA4, GUSB, HLA-DOA, HLA-F, HLA-J, HMBS, IDH1, IFNA2, IGF1, IGFBP3, IL1A, IL1B, IL2, IL3RA, IL10, ITGAM, LAMC2, SMAD4, MECP2, MPO, MSX1, MYH11, NF2, NPM1, NTRK1, OPRD1, PAX2, PDGFRA, PECAM1, PGR, ABCB1, PIK3CA, PIK3CG, PML, PMP22, PRKCZ, PSPH, PXMP2, RANBP2, RING1, BRD2, RPS14, RRAS, S100B, SDHD, SKI, SLC6A4, SMARCA2, SOD1, STAT1, STAT5A, STAT5B, TARBP2, TBX5, TERT, TFAP2A, TFPI, THY1, TIMP3, TOP2A, TPT1, TNFRSF4, TYRO3, KDM6A, VDR, VIM, VIPR2, MOGS, CLLS2, CDK5R1, CD163, EDIL3, RASA4, SLC25A15, LRRC17, EFS, DDX17, CDC42EP3, PTGES3, CHL1, NES, TMED10, EPB41L3, TBC1D9, JPT1, ZBTB7A, TET2, CHD7, CNDP2, LXN, SLC12A9, PDXP, AVEN, XPO5, PCDH10, MRTFA, ACTR6, RBM15, BIRC7, SYVN1, GLIS2, SHANK3, DERL3, RBM45, CREBRF, CNKSR3, TMED10P1, LIN28B, OCM, MIR595, MIR92B, MLSM7, H3P17
Monosomy is a form of aneuploidy with the presence of only one chromosome from a pair. Partial monosomy occurs when a portion of one chromosome in a pair is missing.
Human conditions due to monosomy:
- Turner syndrome – People with Turner syndrome typically have one X chromosome instead of the usual two sex chromosomes. Turner syndrome is the only full monosomy that is seen in humans — all other cases of full monosomy are lethal and the individual will not survive development.
- Cri du chat syndrome – (French for "cry of the cat" after the distinctive noise by affected persons' malformed larynx) a partial monosomy caused by a deletion of the end of the short arm of chromosome 5
- 1p36 deletion syndrome – a partial monosomy caused by a deletion at the end of the short arm of chromosome 1
- Anaphase lag