A Database of Epigenetic Modifiers
Protein: WHSC1L1 |
| Expand All | Collapse All |
| # | Cell Line/Tumor sample | Tissue of Origin | cDNA change | Protein change | Source | FATHMM Prediction | PolyPhen2 Prediction |
|---|---|---|---|---|---|---|---|
| 1 | 2313287 | STOMACH | c.1581_splice | p.K527_splice | CCLE | NP | NP |
| 2 | A204 | SOFT TISSUE | c.119T>C | p.I40T | CCLE | PASSENGER/OTHER | Benign |
| 3 | BICR18 | UPPER AERODIGESTIVE TRACT | c.3558G>C | p.L1186F | CCLE | PASSENGER/OTHER | Probably Damaging |
| 4 | CAL12T | LUNG | c.2660A>G | p.Y887C | CCLE | PASSENGER/OTHER | Possibly Damaging |
| 5 | CL14 | LARGE INTESTINE | c.3925_3926insAAGA | p.R1309fs | CCLE | NP | NP |
| 6 | COLO775 | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.597A>C | p.K199N | CCLE | PASSENGER/OTHER | Probably Damaging |
| 7 | DANG | PANCREAS | c.1409G>C | p.W470S | CCLE | PASSENGER/OTHER | Probably Damaging |
| 8 | DV90 | LUNG | c.1809G>T | p.Q603H | CCLE | PASSENGER/OTHER | Probably Damaging |
| 9 | EN | ENDOMETRIUM | c.3197_3198insA | p.N1066fs | CCLE | NP | NP |
| 10 | EN | ENDOMETRIUM | c.3734T>C | p.L1245P | CCLE | PASSENGER/OTHER | Probably Damaging |
| 11 | FU97 | STOMACH | c.1808A>C | p.Q603P | CCLE | PASSENGER/OTHER | Probably Damaging |
| 12 | GSS | STOMACH | c.3455C>T | p.T1152M | CCLE | PASSENGER/OTHER | Probably Damaging |
| 13 | HCC1569 | BREAST | c.2758G>T | p.G920C | CCLE | PASSENGER/OTHER | Probably Damaging |
| 14 | HEC1B | ENDOMETRIUM | c.587A>G | p.K196R | CCLE | PASSENGER/OTHER | Benign |
| 15 | HEC251 | ENDOMETRIUM | c.2869A>C | p.K957Q | CCLE | PASSENGER/OTHER | Probably Damaging |
| 16 | HEC251 | ENDOMETRIUM | c.4268A>C | p.K1423T | CCLE | PASSENGER/OTHER | Benign |
| 17 | HEC265 | ENDOMETRIUM | c.1708G>T | p.G570C | CCLE | PASSENGER/OTHER | Probably Damaging |
| 18 | HEC265 | ENDOMETRIUM | c.381_382insA | p.K127fs | CCLE | NP | NP |
| 19 | HEC6 | ENDOMETRIUM | c.3859C>T | p.R1287W | CCLE | PASSENGER/OTHER | Probably Damaging |
| 20 | HS888T | BONE | c.3278C>T | p.S1093L | CCLE | PASSENGER/OTHER | Probably Damaging |
| 21 | HT115 | LARGE INTESTINE | c.1531A>G | p.N511D | CCLE | PASSENGER/OTHER | Possibly Damaging |
| 22 | IPC298 | SKIN | c.2115_splice | p.Q705_splice | CCLE | NP | NP |
| 23 | IPC298 | SKIN | c.3830C>G | p.A1277G | CCLE | PASSENGER/OTHER | Benign |
| 24 | JHUEM1 | ENDOMETRIUM | c.1255_1255delA | p.T419fs | CCLE | NP | NP |
| 25 | KYSE410 | OESOPHAGUS | c.1876T>C | p.S626P | CCLE | PASSENGER/OTHER | Probably Damaging |
| 26 | MDAPCA2B | PROSTATE | c.3521A>G | p.Y1174C | CCLE | PASSENGER/OTHER | Probably Damaging |
| 27 | MEG01 | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.1225A>G | p.S409G | CCLE | PASSENGER/OTHER | Benign |
| 28 | MUTZ5 | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.779C>A | p.T260K | CCLE | PASSENGER/OTHER | Benign |
| 29 | NALM6 | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.1904G>A | p.R635H | CCLE | PASSENGER/OTHER | Probably Damaging |
| 30 | NALM6 | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.2693G>A | p.R898H | CCLE | PASSENGER/OTHER | Probably Damaging |
| 31 | NCIH1437 | LUNG | c.1081C>T | p.P361S | CCLE | PASSENGER/OTHER | Possibly Damaging |
| 32 | NCIH1568 | LUNG | c.892A>G | p.T298A | CCLE | PASSENGER/OTHER | Benign |
| 33 | NCIH1944 | LUNG | c.4151C>G | p.S1384* | CCLE | NP | NP |
| 34 | NCIH196 | LUNG | c.3547G>A | p.E1183K | CCLE | PASSENGER/OTHER | Probably Damaging |
| 35 | NCIH2228 | LUNG | c.1328_1329insT | p.S443fs | CCLE | NP | NP |
| 36 | NCIH526 | LUNG | c.1055A>G | p.E352G | CCLE | PASSENGER/OTHER | Probably Damaging |
| 37 | NCIH810 | LUNG | c.1259G>T | p.R420L | CCLE | PASSENGER/OTHER | Probably Damaging |
| 38 | NUGC3 | STOMACH | c.2335G>A | p.V779I | CCLE | PASSENGER/OTHER | Possibly Damaging |
| 39 | OV56 | OVARY | c.3212C>T | p.P1071L | CCLE | PASSENGER/OTHER | Probably Damaging |
| 40 | P12ICHIKAWA | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.1768T>G | p.S590A | CCLE | PASSENGER/OTHER | Possibly Damaging |
| 41 | SNU175 | LARGE INTESTINE | c.2447T>C | p.M816T | CCLE | PASSENGER/OTHER | Possibly Damaging |
| 42 | SNU81 | LARGE INTESTINE | c.1271C>A | p.S424Y | CCLE | PASSENGER/OTHER | Benign |
| 43 | SNUC2A | LARGE INTESTINE | c.3197_3197delA | p.N1066fs | CCLE | NP | NP |
| 44 | SW1710 | URINARY TRACT | c.1015T>A | p.L339I | CCLE | PASSENGER/OTHER | Probably Damaging |
| 45 | SW48 | LARGE INTESTINE | c.3905_3905delA | p.N1302fs | CCLE | NP | NP |
| 46 | VMRCLCD | LUNG | c.2729C>A | p.S910* | CCLE | NP | NP |
| 47 | WM1799 | SKIN | c.2339G>A | p.R780H | CCLE | PASSENGER/OTHER | Probably Damaging |
| 48 | 107106 | BREAST | c.1444T>C | p.S482P | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 49 | 587222 | LARGE INTESTINE | c.736G>T | p.E246* | COSMIC | NP | NP |
| 50 | 587284 | LARGE INTESTINE | c.631C>T | p.R211C | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 51 | 587376 | LARGE INTESTINE | c.1690G>T | p.A564S | COSMIC | PASSENGER/OTHER | Benign |
| 52 | CLL109 | HAEMATOPOIETIC AND LYMPHOID TISSUE | c.550G>A | p.E184K | COSMIC | PASSENGER/OTHER | Benign |
| 53 | ESO-151 | OESOPHAGUS | c.1261C>T | p.R421* | COSMIC | NP | NP |
| 54 | HCC69T | LIVER | c.977G>C | p.R326P | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 55 | HN_62426 | UPPER AERODIGESTIVE TRACT | c.1910C>T | p.S637F | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 56 | LUAD-LIP77 | LUNG | c.721G>T | p.E241* | COSMIC | NP | NP |
| 57 | PD4134a | BREAST | c.1192C>A | p.Q398K | COSMIC | PASSENGER/OTHER | Benign |
| 58 | PD4252a | NS | c.196C>G | p.L66V | COSMIC | PASSENGER/OTHER | Possibly Damaging |
| 59 | RK107_C01 | LIVER | c.1594A>T | p.K532* | COSMIC | NP | NP |
| 60 | TCGA-21-5784-01 | LUNG | c.1126G>A | p.E376K | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 61 | TCGA-24-2288-01 | OVARY | c.824G>C | p.W275S | COSMIC | CANCER | Probably Damaging |
| 62 | TCGA-33-4538-01 | LUNG | c.1552T>C | p.F518L | COSMIC | PASSENGER/OTHER | Benign |
| 63 | TCGA-39-5016-01 | LUNG | c.960G>T | p.A320A | COSMIC | NP | NP |
| 64 | TCGA-39-5030-01 | LUNG | c.1336G>C | p.E446Q | COSMIC | PASSENGER/OTHER | Possibly Damaging |
| 65 | TCGA-55-1594-01 | LUNG | c.632G>A | p.R211H | COSMIC | PASSENGER/OTHER | Benign |
| 66 | TCGA-66-2768-01 | LUNG | c.121G>A | p.A41T | COSMIC | PASSENGER/OTHER | Benign |
| 67 | TCGA-66-2785-01 | LUNG | c.1309G>C | p.E437Q | COSMIC | PASSENGER/OTHER | Benign |
| 68 | TCGA-66-2789-01 | LUNG | c.86G>A | p.R29H | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 69 | TCGA-73-4668-01 | LUNG | c.1306G>T | p.G436W | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 70 | TCGA-91-6831-01 | LUNG | c.933G>A | p.Q311Q | COSMIC | NP | NP |
| 71 | TCGA-A3-3357-01 | KIDNEY | c.928G>T | p.V310F | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 72 | TCGA-A5-A0GI-01 | ENDOMETRIUM | c.261G>A | p.Q87Q | COSMIC | NP | NP |
| 73 | TCGA-AA-3555-01 | LARGE INTESTINE | c.1553T>G | p.F518C | COSMIC | PASSENGER/OTHER | Possibly Damaging |
| 74 | TCGA-AA-A022-01 | LARGE INTESTINE | c.1667C>T | p.T556M | COSMIC | PASSENGER/OTHER | Possibly Damaging |
| 75 | TCGA-AP-A051-01 | ENDOMETRIUM | c.838A>C | p.T280P | COSMIC | PASSENGER/OTHER | Benign |
| 76 | TCGA-AP-A056-01 | ENDOMETRIUM | c.1295A>C | p.Q432P | COSMIC | PASSENGER/OTHER | Benign |
| 77 | TCGA-AP-A056-01 | ENDOMETRIUM | c.1722G>T | p.K574N | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 78 | TCGA-AP-A056-01 | ENDOMETRIUM | c.747A>G | p.P249P | COSMIC | NP | NP |
| 79 | TCGA-AX-A063-01 | ENDOMETRIUM | c.1168T>C | p.Y390H | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 80 | TCGA-AX-A0J0-01 | ENDOMETRIUM | c.1221A>C | p.K407N | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 81 | TCGA-AX-A0J0-01 | ENDOMETRIUM | c.806A>G | p.Q269R | COSMIC | PASSENGER/OTHER | Benign |
| 82 | TCGA-AZ-4315-01 | LARGE INTESTINE | c.115G>A | p.D39N | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 83 | TCGA-B0-5094-01 | KIDNEY | c.1418C>T | p.A473V | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 84 | TCGA-B5-A0JZ-01 | ENDOMETRIUM | c.1194G>A | p.Q398Q | COSMIC | NP | NP |
| 85 | TCGA-B5-A0K6-01 | ENDOMETRIUM | c.701T>C | p.V234A | COSMIC | PASSENGER/OTHER | Benign |
| 86 | TCGA-B5-A11Z-01 | ENDOMETRIUM | c.1010A>C | p.E337A | COSMIC | PASSENGER/OTHER | Possibly Damaging |
| 87 | TCGA-CA-6717-01 | LARGE INTESTINE | c.1136T>C | p.L379S | COSMIC | PASSENGER/OTHER | Probably Damaging |
| 88 | cSCCP8 | SKIN | c.1541G>A | p.G514E | COSMIC | PASSENGER/OTHER | Benign |
| 89 | ccRCC-12 | KIDNEY | c.594A>T | p.K198N | COSMIC | PASSENGER/OTHER | Possibly Damaging |
| 90 | pfg008T | STOMACH | c.1255delA | p.T419fs*8 | COSMIC | NP | NP |
|
|
|
|
| S. No. | Position | Amino acid | Type |
| 1 | 1065 | K | Ubiquitylation |
| 2 | 1391 | K | Acetylation |
| 3 | 1406 | S | Phosphorylation |
| 4 | 1415 | S | Phosphorylation |
| 5 | 150 | S | Phosphorylation |
| 6 | 424 | S | Phosphorylation |
| 7 | 556 | T | Phosphorylation |
| 8 | 556 | T | Phosphorylation |
| 9 | 561 | S | Phosphorylation |
| 10 | 571 | S | Phosphorylation |
| 11 | 571 | S | Phosphorylation |
| 12 | 587 | S | Phosphorylation |
| 13 | 590 | S | Phosphorylation |
| 14 | 637 | S | Phosphorylation |
| 15 | 638 | T | Phosphorylation |
| 16 | 671 | S | Phosphorylation |
| 17 | 790 | K | Acetylation |
| 18 | 790 | K | Acetylation |
| Proteomics DB | COSMIC | Gene Atlas | STRING | PIR |
| WHSC1L1 | WHSC1L1 | WHSC1L1 | ENSP00000313410 | Q9BZ95 |
| QuickGO | HGNC | Ensembl Genome Browser | TreeFam | UniProt |
| Q9BZ95 | WHSC1L1 | ENSP00000313410 | WHSC1L1 | Q9BZ95 |
| Expression Atlas | Protein Atlas | OMIM | IntAct | PharmGKB |
| WHSC1L1 | ENSP00000313410 | 607083 | Q9BZ95 |