| Gene ID | 9219 |
| Symbol | MTA2 |
| Synonymous | MTA1L1|PID |
| Full name | metastasis associated 1 family, member 2 |
| Gene description | MTA1-L1 protein|metastasis -associated gene 1-like 1|metastasis associated gene family, member 2|metastasis-associated 1-like 1|metastasis-associated protein 2|metastasis-associated protein MTA2|p53 target protein in deacetylase complex |
| Cytoband | 11q12-q13.1 |
| Gene type | protein-coding |
| Synonymous | MIM:603947; HGNC:HGNC:7411; Ensembl:ENSG00000149480; HPRD:07233; Vega:OTTHUMG00000167684 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.881T>C; p.F294S; 11:62596638-62596638 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.466G>T; p.E156*; 11:62598048-62598048 |
thyroid | other; neoplasm | Substitution - Nonsense |
c.1409G>T; p.R470M; 11:62595338-62595338 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.385delT; p.Y129fs*33; 11:62598129-62598129 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.479G>A; p.R160H; 11:62598035-62598035 |
large_intestine; colon | NS | Substitution - Missense |
c.385delT; p.Y129fs*33; 11:62598129-62598129 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1678C>T; p.R560W; 11:62594530-62594530 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.299C>T; p.T100I; 11:62598531-62598531 |
skin; arm | malignant_melanoma | Substitution - Missense |
c.307C>T; p.R103W; 11:62598523-62598523 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1683C>T; p.A561A; 11:62594525-62594525 |
skin | malignant_melanoma | Substitution - coding silent |
c.307C>T; p.R103W; 11:62598523-62598523 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.430C>T; p.Q144*; 11:62598084-62598084 |
breast | carcinoma | Substitution - Nonsense |
c.1986G>A; p.E662E; 11:62593896-62593896 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1603C>T; p.P535S; 11:62594605-62594605 |
skin | malignant_melanoma | Substitution - Missense |
c.1718C>T; p.S573F; 11:62594382-62594382 |
skin | malignant_melanoma | Substitution - Missense |
c.1016+5G>A; p.?; 11:62596274-62596274 |
liver | carcinoma | Unknown |
c.1016+5G>A; p.?; 11:62596274-62596274 |
liver | carcinoma | Unknown |
c.1609G>A; p.G537S; 11:62594599-62594599 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.93C>T; p.N31N; 11:62600625-62600625 |
skin | malignant_melanoma | Substitution - coding silent |
c.1382T>C; p.L461P; 11:62595365-62595365 |
lung; left_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1906C>T; p.L636L; 11:62593976-62593976 |
skin | malignant_melanoma | Substitution - coding silent |
c.1507G>A; p.A503T; 11:62595047-62595047 |
skin; head_neck | malignant_melanoma; superficial_spreading | Substitution - Missense |
c.1017-1G>A; p.?; 11:62596108-62596108 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.1068G>A; p.M356I; 11:62596056-62596056 |
breast | carcinoma | Substitution - Missense |
c.1017-1G>A; p.?; 11:62596108-62596108 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.823C>T; p.L275L; 11:62596696-62596696 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.910G>T; p.V304F; 11:62596505-62596505 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.82G>C; p.E28Q; 11:62600636-62600636 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1438C>T; p.R480*; 11:62595309-62595309 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.188C>T; p.A63V; 11:62600168-62600168 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.188C>T; p.A63V; 11:62600168-62600168 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.354C>T; p.S118S; 11:62598345-62598345 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.373G>T; p.D125Y; 11:62598141-62598141 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.373G>T; p.D125Y; 11:62598141-62598141 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.337G>T; p.E113*; 11:62598362-62598362 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1493G>A; p.R498Q; 11:62595061-62595061 |
liver | carcinoma | Substitution - Missense |
c.694-1G>C; p.?; 11:62596826-62596826 |
ovary | carcinoma; serous_carcinoma | Unknown |
c.1493G>A; p.R498Q; 11:62595061-62595061 |
liver | carcinoma | Substitution - Missense |
c.790G>A; p.E264K; 11:62596729-62596729 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.343G>C; p.D115H; 11:62598356-62598356 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.570C>T; p.I190I; 11:62597633-62597633 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.457T>C; p.Y153H; 11:62598057-62598057 |
skin | malignant_melanoma | Substitution - Missense |
c.438G>A; p.E146E; 11:62598076-62598076 |
breast | carcinoma | Substitution - coding silent |
c.139C>T; p.R47W; 11:62600217-62600217 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1600delA; p.T534fs*25; 11:62594608-62594608 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.222G>C; p.G74G; 11:62598608-62598608 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1323C>T; p.A441A; 11:62595424-62595424 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1913T>G; p.V638G; 11:62593969-62593969 |
breast | carcinoma | Substitution - Missense |
c.656A>C; p.H219P; 11:62597353-62597353 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1070A>G; p.N357S; 11:62596054-62596054 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1321G>A; p.A441T; 11:62595426-62595426 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1531C>T; p.P511S; 11:62595023-62595023 |
skin | malignant_melanoma | Substitution - Missense |
c.657C>G; p.H219Q; 11:62597352-62597352 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1889G>C; p.R630P; 11:62593993-62593993 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1151C>G; p.P384R; 11:62595855-62595855 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1846C>A; p.L616I; 11:62594036-62594036 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.406G>A; p.V136M; 11:62598108-62598108 |
prostate | carcinoma | Substitution - Missense |
c.1176T>G; p.A392A; 11:62595830-62595830 |
skin | malignant_melanoma | Substitution - coding silent |
c.238C>T; p.R80C; 11:62598592-62598592 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.325A>G; p.T109A; 11:62598374-62598374 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.718delA; p.R240fs*41; 11:62596801-62596801 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.1965A>C; p.S655S; 11:62593917-62593917 |
thyroid | other; neoplasm | Substitution - coding silent |
c.1142G>A; p.W381*; 11:62595864-62595864 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1923G>A; p.T641T; 11:62593959-62593959 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.256C>A; p.R86R; 11:62598574-62598574 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.373-6T>C; p.?; 11:62598147-62598147 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Unknown |
c.1843G>C; p.A615P; 11:62594039-62594039 |
prostate | carcinoma | Substitution - Missense |
c.1375A>G; p.T459A; 11:62595372-62595372 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1232A>G; p.E411G; 11:62595774-62595774 |
prostate | adenoma | Substitution - Missense |
c.809C>T; p.A270V; 11:62596710-62596710 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.809C>T; p.A270V; 11:62596710-62596710 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.809C>T; p.A270V; 11:62596710-62596710 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.809C>T; p.A270V; 11:62596710-62596710 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.301delC; p.H101fs*8; 11:62598529-62598529 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1041C>T; p.I347I; 11:62596083-62596083 |
skin | malignant_melanoma | Substitution - coding silent |
c.1463C>T; p.A488V; 11:62595284-62595284 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.92A>G; p.N31S; 11:62600626-62600626 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1298G>A; p.S433N; 11:62595449-62595449 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1488C>T; p.S496S; 11:62595066-62595066 |
skin | malignant_melanoma | Substitution - coding silent |
c.122A>C; p.K41T; 11:62600234-62600234 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.421C>T; p.L141F; 11:62598093-62598093 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.848A>G; p.Y283C; 11:62596671-62596671 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myeloid_leukaemia | Substitution - Missense |
c.848A>G; p.Y283C; 11:62596671-62596671 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myeloid_leukaemia | Substitution - Missense |
c.339G>T; p.E113D; 11:62598360-62598360 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1453C>T; p.P485S; 11:62595294-62595294 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.1357A>C; p.T453P; 11:62595390-62595390 |
thyroid | other; neoplasm | Substitution - Missense |
c.1567G>T; p.D523Y; 11:62594987-62594987 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.889T>C; p.W297R; 11:62596526-62596526 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.133C>T; p.L45F; 11:62600223-62600223 |
skin | malignant_melanoma | Substitution - Missense |
c.1578C>T; p.A526A; 11:62594630-62594630 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1874T>G; p.M625R; 11:62594008-62594008 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.1664delG; p.G555fs*4; 11:62594544-62594544 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1664delG; p.G555fs*4; 11:62594544-62594544 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1936C>T; p.R646W; 11:62593946-62593946 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.221G>A; p.G74E; 11:62598609-62598609 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.221G>A; p.G74E; 11:62598609-62598609 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.1853A>G; p.K618R; 11:62594029-62594029 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1850G>A; p.R617Q; 11:62594032-62594032 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.405C>T; p.P135P; 11:62598109-62598109 |
pancreas | carcinoma | Substitution - coding silent |
c.405C>T; p.P135P; 11:62598109-62598109 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1916A>C; p.K639T; 11:62593966-62593966 |
thyroid | other; neoplasm | Substitution - Missense |
c.982G>C; p.D328H; 11:62596313-62596313 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.319A>T; p.S107C; 11:62598380-62598380 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1746G>C; p.G582G; 11:62594354-62594354 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.311G>A; p.G104E; 11:62598388-62598388 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.311G>A; p.G104E; 11:62598388-62598388 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1832A>T; p.K611M; 11:62594268-62594268 |
pancreas | pancreatic_intraepithelial_neoplasia_(PanIN) | Substitution - Missense |
c.1832A>T; p.K611M; 11:62594268-62594268 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1255-2A>G; p.?; 11:62595494-62595494 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.1994T>A; p.V665D; 11:62593888-62593888 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1996C>T; p.L666L; 11:62593886-62593886 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1782G>A; p.Q594Q; 11:62594318-62594318 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1442G>A; p.R481Q; 11:62595305-62595305 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1664_1665insG; p.I556fs*8; 11:62594543-62594544 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.765G>T; p.Q255H; 11:62596754-62596754 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1560C>T; p.I520I; 11:62594994-62594994 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.785G>A; p.R262Q; 11:62596734-62596734 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.785G>A; p.R262Q; 11:62596734-62596734 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.2005T>A; p.*669R; 11:62593877-62593877 |
stomach | carcinoma; adenocarcinoma | Nonstop extension |
c.593+9T>G; p.?; 11:62597601-62597601 |
ovary | other; neoplasm | Unknown |
c.534C>T; p.V178V; 11:62597669-62597669 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.317G>A; p.C106Y; 11:62598382-62598382 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.435C>T; p.G145G; 11:62598079-62598079 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.866A>G; p.D289G; 11:62596653-62596653 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1701G>A; p.G567G; 11:62594399-62594399 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |