| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 7103 |
Name | TSPAN8 |
Synonymous | tetraspanin 8;TSPAN8;tetraspanin 8 |
Definition | tetraspanin-8|transmembrane 4 superfamily member 3|tspan-8|tumor-associated antigen CO-029 |
Position | 12q14.1-q21.1 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.403G>A; p.E135K; 12:71137994-71137994 |
skin | malignant_melanoma | Substitution - Missense |
c.403G>A; p.E135K; 12:71137994-71137994 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.656T>C; p.I219T; 12:71129335-71129335 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.388G>A; p.A130T; 12:71138009-71138009 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.485G>A; p.G162E; 12:71132784-71132784 |
skin | malignant_melanoma | Substitution - Missense |
c.444G>A; p.E148E; 12:71137953-71137953 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.468T>A; p.N156K; 12:71132801-71132801 |
breast | carcinoma | Substitution - Missense |
c.302C>T; p.A101V; 12:71138190-71138190 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.210C>T; p.G70G; 12:71139762-71139762 |
skin | malignant_melanoma | Substitution - coding silent |
c.136G>A; p.E46K; 12:71139836-71139836 |
skin | malignant_melanoma | Substitution - Missense |
c.336+1G>A; p.?; 12:71138155-71138155 |
skin | malignant_melanoma | Unknown |
c.222C>T; p.C74C; 12:71139750-71139750 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.222C>T; p.C74C; 12:71139750-71139750 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.407A>T; p.K136I; 12:71137990-71137990 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.506C>T; p.P169L; 12:71132763-71132763 |
skin | malignant_melanoma | Substitution - Missense |
c.124-2A>C; p.?; 12:71139850-71139850 |
lung | carcinoma; small_cell_carcinoma | Unknown |
c.124-2A>C; p.?; 12:71139850-71139850 |
lung | carcinoma; small_cell_carcinoma | Unknown |
c.78C>T; p.I26I; 12:71144196-71144196 |
skin | malignant_melanoma | Substitution - coding silent |
c.51C>T; p.F17F; 12:71157628-71157628 |
skin; trunk | malignant_melanoma; nodular | Substitution - coding silent |
c.74T>C; p.L25S; 12:71144200-71144200 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.74T>C; p.L25S; 12:71144200-71144200 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.675G>A; p.V225V; 12:71125373-71125373 |
breast | carcinoma | Substitution - coding silent |
c.496C>G; p.Q166E; 12:71132773-71132773 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.109A>C; p.N37H; 12:71144165-71144165 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.20G>A; p.C7Y; 12:71157659-71157659 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.51C>A; p.F17L; 12:71157628-71157628 |
liver | carcinoma | Substitution - Missense |
c.51C>A; p.F17L; 12:71157628-71157628 |
liver | carcinoma | Substitution - Missense |
c.149C>T; p.S50F; 12:71139823-71139823 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.699G>A; p.Q233Q; 12:71125349-71125349 |
skin | malignant_melanoma | Substitution - coding silent |
c.427A>C; p.I143L; 12:71137970-71137970 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.396G>A; p.G132G; 12:71138001-71138001 |
skin | malignant_melanoma | Substitution - coding silent |
c.29_31delATT; p.Y10delY; 12:71157648-71157650 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.256C>T; p.L86L; 12:71139716-71139716 |
skin | malignant_melanoma | Substitution - coding silent |
c.112G>A; p.D38N; 12:71144162-71144162 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.124-2A>G; p.?; 12:71139850-71139850 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.489T>G; p.N163K; 12:71132780-71132780 |
skin | malignant_melanoma | Substitution - Missense |
c.238G>A; p.E80K; 12:71139734-71139734 |
skin | malignant_melanoma | Substitution - Missense |
c.176T>C; p.L59S; 12:71139796-71139796 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.625G>C; p.V209L; 12:71129366-71129366 |
oesophagus | carcinoma | Substitution - Missense |
c.645A>G; p.G215G; 12:71129346-71129346 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.218G>C; p.G73A; 12:71139754-71139754 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.218G>C; p.G73A; 12:71139754-71139754 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.218G>C; p.G73A; 12:71139754-71139754 |
kidney | other; neoplasm | Substitution - Missense |
c.623T>G; p.I208R; 12:71129368-71129368 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.245G>A; p.R82H; 12:71139727-71139727 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.130G>A; p.G44S; 12:71139842-71139842 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.130G>A; p.G44S; 12:71139842-71139842 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.699G>T; p.Q233H; 12:71125349-71125349 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.589T>C; p.F197L; 12:71129402-71129402 |
skin | malignant_melanoma | Substitution - Missense |
c.126T>A; p.I42I; 12:71139846-71139846 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.694T>G; p.C232G; 12:71125354-71125354 |
skin | malignant_melanoma | Substitution - Missense |
c.261+1G>A; p.?; 12:71139710-71139710 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.577-6delT; p.?; 12:71129420-71129420 |
stomach | carcinoma; diffuse_adenocarcinoma | Unknown |
c.482G>T; p.W161L; 12:71132787-71132787 |
breast | carcinoma | Substitution - Missense |
c.182C>T; p.A61V; 12:71139790-71139790 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.539C>T; p.P180L; 12:71132730-71132730 |
skin | malignant_melanoma | Substitution - Missense |
c.382T>C; p.L128L; 12:71138015-71138015 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.414C>T; p.F138F; 12:71137983-71137983 |
skin | malignant_melanoma | Substitution - coding silent |
c.414C>T; p.F138F; 12:71137983-71137983 |
skin; arm | malignant_melanoma | Substitution - coding silent |
c.557G>A; p.G186E; 12:71132712-71132712 |
skin | malignant_melanoma | Substitution - Missense |
c.557G>A; p.G186E; 12:71132712-71132712 |
skin | malignant_melanoma | Substitution - Missense |
c.557G>A; p.G186E; 12:71132712-71132712 |
skin | malignant_melanoma | Substitution - Missense |
c.513A>C; p.L171F; 12:71132756-71132756 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.513A>C; p.L171F; 12:71132756-71132756 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.684G>T; p.M228I; 12:71125364-71125364 |
thyroid | carcinoma | Substitution - Missense |
c.456C>T; p.C152C; 12:71132813-71132813 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.343C>T; p.R115C; 12:71138054-71138054 |
skin; neck | malignant_melanoma | Substitution - Missense |
c.465C>T; p.V155V; 12:71132804-71132804 |
skin | malignant_melanoma | Substitution - coding silent |
c.465C>T; p.V155V; 12:71132804-71132804 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.243T>A; p.S81R; 12:71139729-71139729 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.574G>C; p.E192Q; 12:71132695-71132695 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.189T>G; p.G63G; 12:71139783-71139783 |
breast | carcinoma | Substitution - coding silent |
c.577-1G>A; p.?; 12:71129415-71129415 |
breast | carcinoma | Unknown |
c.591C>T; p.F197F; 12:71129400-71129400 |
skin | malignant_melanoma | Substitution - coding silent |
c.453C>T; p.C151C; 12:71132816-71132816 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.34A>G; p.M12V; 12:71157645-71157645 |
ovary | other; neoplasm | Substitution - Missense |
c.116C>T; p.S39F; 12:71144158-71144158 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.394G>A; p.G132R; 12:71138003-71138003 |
skin | malignant_melanoma | Substitution - Missense |