| Gene ID | 643 |
| Symbol | CXCR5 |
| Synonymous | BLR1|CD185|MDR15 |
| Full name | chemokine (C-X-C motif) receptor 5 |
| Gene description | Burkitt lymphoma receptor 1, GTP binding protein (chemokine (C-X-C motif) receptor 5)|Burkitt lymphoma receptor 1, GTP-binding protein|C-X-C chemokine receptor type 5|CXC-R5|CXCR-5|MDR-15|monocyte-derived receptor 15 |
| Cytoband | 11q23.3 |
| Gene type | protein-coding |
| Synonymous | MIM:601613; HGNC:HGNC:1060; HPRD:03367 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.258G>A; p.T86T; 11:118893802-118893802 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1048C>T; p.Q350*; 11:118894592-118894592 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; follicular_lymphoma | Substitution - Nonsense |
c.3G>T; p.M1I; 11:118883944-118883944 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1067G>A; p.R356H; 11:118894611-118894611 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.439C>T; p.R147C; 11:118893983-118893983 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.782C>T; p.A261V; 11:118894326-118894326 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.902C>T; p.P301L; 11:118894446-118894446 |
skin | malignant_melanoma | Substitution - Missense |
c.602G>A; p.R201H; 11:118894146-118894146 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.151G>A; p.A51T; 11:118893695-118893695 |
skin | malignant_melanoma | Substitution - Missense |
c.1089_1090delAG; p.N365fs*>8; 11:118894633-118894634 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.988C>T; p.R330C; 11:118894532-118894532 |
pancreas | carcinoma; acinar_carcinoma | Substitution - Missense |
c.54C>T; p.F18F; 11:118893598-118893598 |
breast | carcinoma | Substitution - coding silent |
c.85G>A; p.D29N; 11:118893629-118893629 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.85G>A; p.D29N; 11:118893629-118893629 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.831C>T; p.I277I; 11:118894375-118894375 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.762G>A; p.R254R; 11:118894306-118894306 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.165C>T; p.P55P; 11:118893709-118893709 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.854C>T; p.A285V; 11:118894398-118894398 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.854C>T; p.A285V; 11:118894398-118894398 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.528_529GG>AA; p.G177S; 11:118894072-118894073 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1044G>A; p.L348L; 11:118894588-118894588 |
pituitary; craniopharyngeal_duct | craniopharyngioma; adamantinomatous | Substitution - coding silent |
c.1002G>A; p.S334S; 11:118894546-118894546 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.978C>T; p.G326G; 11:118894522-118894522 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.558C>A; p.L186L; 11:118894102-118894102 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.655C>T; p.R219*; 11:118894199-118894199 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1119G>C; p.*373Y; 11:118894663-118894663 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Nonstop extension |
c.117T>G; p.P39P; 11:118893661-118893661 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.562G>A; p.A188T; 11:118894106-118894106 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.578G>A; p.G193D; 11:118894122-118894122 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.126delG; p.L45fs*22; 11:118893670-118893670 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.635C>T; p.T212M; 11:118894179-118894179 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.747G>A; p.Q249Q; 11:118894291-118894291 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.885G>T; p.K295N; 11:118894429-118894429 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.754C>T; p.P252S; 11:118894298-118894298 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.516C>T; p.T172T; 11:118894060-118894060 |
skin | malignant_melanoma | Substitution - coding silent |
c.665A>C; p.Y222S; 11:118894209-118894209 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; follicular_lymphoma | Substitution - Missense |
c.609C>G; p.T203T; 11:118894153-118894153 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1014G>C; p.T338T; 11:118894558-118894558 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1014G>C; p.T338T; 11:118894558-118894558 |
thyroid | other; neoplasm | Substitution - coding silent |
c.433G>A; p.V145M; 11:118893977-118893977 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.989G>A; p.R330H; 11:118894533-118894533 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.477C>T; p.R159R; 11:118894021-118894021 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.257C>T; p.T86M; 11:118893801-118893801 |
prostate | carcinoma | Substitution - Missense |
c.109C>T; p.L37F; 11:118893653-118893653 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.781G>T; p.A261S; 11:118894325-118894325 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.353G>A; p.G118E; 11:118893897-118893897 |
skin | malignant_melanoma | Substitution - Missense |
c.332G>A; p.G111D; 11:118893876-118893876 |
skin | malignant_melanoma | Substitution - Missense |
c.322G>A; p.V108M; 11:118893866-118893866 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1108A>T; p.T370S; 11:118894652-118894652 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.301G>A; p.V101I; 11:118893845-118893845 |
skin | malignant_melanoma | Substitution - Missense |
c.512G>A; p.G171E; 11:118894056-118894056 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.327C>T; p.A109A; 11:118893871-118893871 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.583C>T; p.H195Y; 11:118894127-118894127 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.127G>A; p.G43R; 11:118893671-118893671 |
skin | malignant_melanoma | Substitution - Missense |
c.297G>A; p.L99L; 11:118893841-118893841 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.282C>T; p.A94A; 11:118893826-118893826 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.587A>T; p.N196I; 11:118894131-118894131 |
large_intestine | NS | Substitution - Missense |
c.751C>T; p.R251C; 11:118894295-118894295 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1119G>T; p.*373Y; 11:118894663-118894663 |
lung | carcinoma; small_cell_carcinoma | Nonstop extension |
c.100G>A; p.E34K; 11:118893644-118893644 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.976G>A; p.G326S; 11:118894520-118894520 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.387_388insA; p.V131fs*178; 11:118893931-118893932 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Insertion - Frameshift |
c.561C>T; p.F187F; 11:118894105-118894105 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.475C>T; p.R159C; 11:118894019-118894019 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.36G>A; p.E12E; 11:118883977-118883977 |
skin | malignant_melanoma | Substitution - coding silent |
c.1108A>C; p.T370P; 11:118894652-118894652 |
breast | carcinoma | Substitution - Missense |