Table 7. CIS gene orthologues in human tumors1.
Mouse or Virus Strain | Gene ID | Human Gene Symbol | Gene Ranker Score | Rank out of 7658 | Broad | Cosmic | Vogelstein | Sanger |
---|---|---|---|---|---|---|---|---|
MMTVSP | 2268 | FGR | 1.25 | 2587 | Y | |||
Core | 5156 | PDGFRA | 11 | 11 | Y | Y | Y | Y |
Core | 2248 | FGF3 | 1.25 | 2585 | ||||
Core | 2249 | FGF4 | 1.25 | 2586 | ||||
MMTVSP | 2E+05 | PHACTR1 | 1.5 | 2319 | Y | |||
MMTVCZ & SP | 6383 | SDC2 | 2 | 1741 | ||||
Core | 3E+05 | RSPO2 | 1.5 | 2383 | Y | |||
Core | 7480 | WNT10B | 2.5 | 980 | Y | |||
Core | 7471 | WNT1 | 1.25 | 2829 | Y | |||
MMTVCZ & SP | 4855 | NOTCH4 | 2.75 | 740 | Y | |||
Core | 2253 | FGF8 | 1.5 | 2141 |
The human orthologues of MMTV CIS genes that are at risk of mutation in human cancers as determined by The Cancer Gene Atlas (TCGA) [28, 29]. TCGA is comprised of 39 gene lists containing a total of 7658 genes which have been ranked in part by the number of gene lists on which they appear. Each list that is contributed to Gene Ranker gets a score: [38] and a ranking out of the 7658 genes in the TCGA catalogue. A ranking of less than 3500 is associated with a gene that is at “high risk” for mutation in human cancer. A “Y” indicates that mutations have been found in that particular gene in the Cosmic [30], Sanger [31], Broad 2000 [29] and/or Volgestein/Kinzler [32] databases of mutations identified by nucleotide sequence analysis. The particular mouse or virus strain with which the gene was identified is indicated.