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. 2008 Sep;12(3):183–199. doi: 10.1089/omi.2008.0010

Table 3.

A Clade of All Leiomyosarcoma Specimens Defined by 20 Synapomorphies in Comparison to Normal and Leiomyoma Specimens

A. Overexpressed synapomorphic genes:
X54942 CKS2 CDC28 proteininase regulatory subunit 2 NS
U68566 HAX1 HCLS1 associated protein X-1 NS
L03411 RDBP RD RNA binding protein OE
X59543 RRM1 ribonucleotide reductase M1 polypeptide NS
B. Underexpressed synapomorphic genes:
D13639 CCND2, cyclin D2 UE
D21337 COL4A6 collagen, type IV, alpha 6 UE
 HG2810-HT2921_at Csh2 chorionic somatomammotropin hormone 2 [Rattus norvegicus] NS
L36033 CXCL12 chemokine (C-X-C motif) ligand 12 (stromal cell-derived factor 1) NS
 HG2663-HT2759_at EMX2 empty spiracles homolog 2 (Drosophila). Homeotic Protein Emx2 NS
 HG2663-HT2759_at Homeotic Protein Emx2 NS
 HG2810-HT2921_at HOXA10 homeobox A10 Expressed in the adult human endometrium UE
AB002382 LOC284394 hypothetical gene supported by NM_001331 NS
U69263 MATN2 matrilin 2 UE
U85707 Meis1, myeloid ecotropic viral integration site 1 homolog (mouse) UE
Z29678 MITF microphthalmia-associated transcription factor UE
L35240 PDLIM7 PDZ and LIM domain 7 (enigma) NS
D87735 RL14 ribosomal protein L14 NS
L14076 SFRS4 splicing factor, arginine/serine-rich 4 UE
J05243 SPTAN1 spectrin, alpha, nonerythrocytic 1 (alpha-fodrin) NS
C. Dichotomously-expressed synapomorphic genes:
M33197 GAPDH glyceraldehyde-3-phosphate dehydrogenase NS

Last column reports the status of the synapomorphies as described by Quade et al. (2004) in their significant genes list.