Table 2.
Mutation statuses of 20 genes in the CRC lines in comparison with PDX tumors.
| PDX CRC ID | Bladder PDX ID | PDX CRC ID | Gene Symbol | Transcript ID | CDS mutation (in PDX) | AA Mutation (in PDX) | CDS mutation (in PDX CRCs) |
|---|---|---|---|---|---|---|---|
| CRC958-1 | BL0269F404P0 | CRC269 | FAT4 | NM_001291303.1 | c.1855C>T | p.R619C | c.1855C>T |
| KMT2C | NM_170606.2 | c.9694G>T | p.E3232★ | c.9694G>T | |||
| PIK3CA | NM_006218.2 | c.2176G>A | p.E726K | c.2176G>A | |||
| c.3140A>G | p.H1047R | c.3140A>G | |||||
| KMT2D | NM_003482.3 | c.2438C>T | p.P813L | c.2438C>T | |||
| c.7411C>T | p.R2471★ | c.7411C>T | |||||
| FOXA1 | NM_004496.3 | c.150G>A | p.M50I | c.150G>A | |||
| SYNE1 | NM_182961.3 | c.2653T>G | p.L885V | c.2653T>G | |||
| ZFR2 | NM_015174.1 | c.172G>A | p.G58S | c.172G>A | |||
| ADCY2 | NM_020546.2 | c.439G>T | p.V147L | c.439G>T | |||
| CRC958-2 | BL0269F404P0_GDC-R | CRC269-R | FAT4 | NM_001291303.1 | c.1855C>T | p.R619C | c.1855C>T |
| KMT2C | NM_170606.2 | c.9694G>T | p.E3232★ | c.9694G>T | |||
| PIK3CA | NM_006218.2 | c.2176G>A | p.E726K | c.2176G>A | |||
| c.3140A>G | p.H1047R | c.3140A>G | |||||
| KMT2D | NM_003482.3 | c.2438C>T | p.P813L | c.2438C>T | |||
| c.7411C>T | p.R2471 ★ | c.7411C>T | |||||
| FOXA1 | NM_004496.3 | c.150G>A | p.M50I | c.150G>A | |||
| SYNE1 | NM_182961.3 | c.2653T>G | p.L885V | c.2653T>G | |||
| ZFR2 | NM_015174.1 | c.172G>A | p.G58S | c.172G>A | |||
| ADCY2 | NM_020546.2 | c.439G>T | p.V147L | c.439G>T | |||
| CRC958-3 | BL0293F563P0 | CRC293 | ARID1A | NM_006015.4 | c.413C>G | p.S138★ | c.413C>G |
| TP53 | NM_001126112.2 | c.626G>A | p.R209Q | c.626G # | |||
| c.743G>A | p.R248Q | c.743G>A | |||||
| SYNE2 | NM_015180.4 | c.4177C>T | p.R1393W | c.4177C>T | |||
| EP300 | NM_001429.3 | c.4040G>T | p.G1347V | c.4040G>T | |||
| CDKN2A | NM_000077.4 | c.442G>A | p.A148T | c.442G>A | |||
| MTOR | NM_004958.3 | c.5533G>A | p.E1845K | c.5533G>A | |||
| CRC958-4 | BL0382F1232P0 | CRC382 | ATM | NM 000051.3 | c.5557G>A | p.D1853N | c.5557G>A |
| TP53 | NM_001126112.2 | c.610G>T | p.E204★ | c.610G>T | |||
| c.25G>T | Sense mutation | c.25G>T | |||||
| KLF5 | NM_001730.4 | c.1255G>C | p.E419Q | c.1255G>C | |||
| MERTK | NM_006343.2 | c.878G>A | p.R293H | c.878G>A | |||
| MYH10 | NM_001256012.1 | c.2879C>G | p.S960C | c.2879C>G | |||
| NUP98 | NM_016320.4 | c.3424C>G | p.Q1142E | c.3424C>G | |||
| SETD2 | NM_014159.6 | c.6694C>T | p.P2232S | c.6694C>T |
STOP codon
no mutataion observed