| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 3549 |
Name | IHH |
Synonymous | indian hedgehog;IHH;indian hedgehog |
Definition | HHG-2|Indian hedgehog homolog|indian hedgehog protein |
Position | 2q33-q35 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.655G>A; p.A219T; 2:219055788-219055788 |
skin | malignant_melanoma | Substitution - Missense |
c.292G>A; p.G98S; 2:219060176-219060176 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1044C>T; p.F348F; 2:219055399-219055399 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1044C>T; p.F348F; 2:219055399-219055399 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.19C>T; p.R7W; 2:219060449-219060449 |
skin | malignant_melanoma | Substitution - Missense |
c.632G>A; p.R211H; 2:219055811-219055811 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.892G>A; p.V298M; 2:219055551-219055551 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.851C>T; p.T284M; 2:219055592-219055592 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1131G>A; p.P377P; 2:219055312-219055312 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.665C>T; p.A222V; 2:219055778-219055778 |
central_nervous_system; brain | glioma; astrocytoma_Grade_II | Substitution - Missense |
c.599C>T; p.T200M; 2:219055844-219055844 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1011A>C; p.T337T; 2:219055432-219055432 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.167T>C; p.V56A; 2:219060301-219060301 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.124C>T; p.R42C; 2:219060344-219060344 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.746G>A; p.R249H; 2:219055697-219055697 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.748G>T; p.E250*; 2:219055695-219055695 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.447C>T; p.R149R; 2:219057563-219057563 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.447C>T; p.R149R; 2:219057563-219057563 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1156delC; p.Q386fs*11; 2:219055287-219055287 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1156delC; p.Q386fs*11; 2:219055287-219055287 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1156delC; p.Q386fs*11; 2:219055287-219055287 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1156_1157insC; p.Q386fs*>27; 2:219055286-219055287 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.247C>A; p.P83T; 2:219060221-219060221 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.603C>T; p.G201G; 2:219055840-219055840 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.603C>T; p.G201G; 2:219055840-219055840 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.738C>T; p.F246F; 2:219055705-219055705 |
skin | malignant_melanoma | Substitution - coding silent |
c.647C>T; p.A216V; 2:219055796-219055796 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.444C>T; p.G148G; 2:219057566-219057566 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.559C>T; p.H187Y; 2:219057451-219057451 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.675G>A; p.P225P; 2:219055768-219055768 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.123A>G; p.P41P; 2:219060345-219060345 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.109C>A; p.R37S; 2:219060359-219060359 |
thyroid | other; neoplasm | Substitution - Missense |
c.390C>G; p.T130T; 2:219057620-219057620 |
pancreas | carcinoma | Substitution - coding silent |
c.1175G>A; p.G392E; 2:219055268-219055268 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1129C>T; p.P377S; 2:219055314-219055314 |
skin | malignant_melanoma | Substitution - Missense |
c.670A>G; p.R224G; 2:219055773-219055773 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.218G>A; p.R73H; 2:219060250-219060250 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.838delG; p.A280fs*85; 2:219055605-219055605 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.1138G>A; p.G380S; 2:219055305-219055305 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.990C>T; p.A330A; 2:219055453-219055453 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.503G>A; p.R168H; 2:219057507-219057507 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1063C>T; p.H355Y; 2:219055380-219055380 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.775G>A; p.V259I; 2:219055668-219055668 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.869T>C; p.F290S; 2:219055574-219055574 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.403G>A; p.E135K; 2:219057607-219057607 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.910G>A; p.V304M; 2:219055533-219055533 |
liver | carcinoma | Substitution - Missense |
c.910G>A; p.V304M; 2:219055533-219055533 |
liver | carcinoma | Substitution - Missense |
c.445C>T; p.R149C; 2:219057565-219057565 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.116G>C; p.R39P; 2:219060352-219060352 |
breast | carcinoma | Substitution - Missense |
c.113G>C; p.R38P; 2:219060355-219060355 |
central_nervous_system; brain | glioma; astrocytoma_Grade_II | Substitution - Missense |
c.486G>A; p.K162K; 2:219057524-219057524 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.584C>T; p.S195L; 2:219055859-219055859 |
skin | malignant_melanoma | Substitution - Missense |
c.58C>G; p.L20V; 2:219060410-219060410 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.58C>G; p.L20V; 2:219060410-219060410 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.795C>T; p.P265P; 2:219055648-219055648 |
skin | malignant_melanoma | Substitution - coding silent |
c.781G>A; p.E261K; 2:219055662-219055662 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.909C>T; p.Y303Y; 2:219055534-219055534 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.762G>A; p.L254L; 2:219055681-219055681 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1050C>T; p.A350A; 2:219055393-219055393 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.707G>T; p.G236V; 2:219055736-219055736 |
pancreas | carcinoma | Substitution - Missense |
c.1128T>C; p.T376T; 2:219055315-219055315 |
breast | carcinoma | Substitution - coding silent |
c.1128T>C; p.T376T; 2:219055315-219055315 |
thyroid | other; neoplasm | Substitution - coding silent |
c.600G>A; p.T200T; 2:219055843-219055843 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.762G>C; p.L254L; 2:219055681-219055681 |
breast | carcinoma | Substitution - coding silent |
c.835A>G; p.T279A; 2:219055608-219055608 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.666C>T; p.A222A; 2:219055777-219055777 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.194G>A; p.G65E; 2:219060274-219060274 |
breast | carcinoma | Substitution - Missense |
c.683G>A; p.R228H; 2:219055760-219055760 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.165T>C; p.N55N; 2:219060303-219060303 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.419C>T; p.S140L; 2:219057591-219057591 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.831_832insCCCTGCTC; p.F278fs*90; 2:219055611-219055612 |
endometrium | carcinoma; endometrioid_carcinoma | Insertion - Frameshift |
c.1134_1135GG>AA; p.E379K; 2:219055308-219055309 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.757_760delAGGC; p.R253fs*1; 2:219055683-219055686 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.797delC; p.P266fs*99; 2:219055646-219055646 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.797delC; p.P266fs*99; 2:219055646-219055646 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.429C>A; p.S143S; 2:219057581-219057581 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1136A>G; p.E379G; 2:219055307-219055307 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.648G>A; p.A216A; 2:219055795-219055795 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1135G>A; p.E379K; 2:219055308-219055308 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.667G>A; p.V223M; 2:219055776-219055776 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1135G>A; p.E379K; 2:219055308-219055308 |
skin | malignant_melanoma | Substitution - Missense |
c.1143G>T; p.V381V; 2:219055300-219055300 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.639G>A; p.E213E; 2:219055804-219055804 |
skin | malignant_melanoma | Substitution - coding silent |
c.992C>T; p.P331L; 2:219055451-219055451 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.992C>T; p.P331L; 2:219055451-219055451 |
skin | malignant_melanoma | Substitution - Missense |
c.98T>G; p.V33G; 2:219060370-219060370 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1034C>T; p.A345V; 2:219055409-219055409 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.125G>A; p.R42H; 2:219060343-219060343 |
thyroid | other; neoplasm | Substitution - Missense |
c.943G>A; p.A315T; 2:219055500-219055500 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |