| Gene ID | 2217 |
| Symbol | FCGRT |
| Synonymous | FCRN|alpha-chain |
| Full name | Fc fragment of IgG, receptor, transporter, alpha |
| Gene description | FcRn alpha chain|IgG Fc fragment receptor transporter alpha chain|IgG receptor FcRn large subunit p51|immunoglobulin receptor, intestinal, heavy chain|major histocompatibility complex class I-like Fc receptor|neonatal Fc receptor|neonatal Fc-receptor for |
| Cytoband | 19q13.3 |
| Gene type | protein-coding |
| Synonymous | MIM:601437; HGNC:HGNC:3621; Ensembl:ENSG00000104870; HPRD:03257; Vega:OTTHUMG00000183155 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.621G>A; p.L207L; 19:49524526-49524526 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.204G>A; p.A68A; 19:49514012-49514012 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1093G>A; p.A365T; 19:49526114-49526114 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.328C>T; p.P110S; 19:49514213-49514213 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.779C>T; p.S260L; 19:49524684-49524684 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.305T>A; p.F102Y; 19:49514113-49514113 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.525C>T; p.L175L; 19:49514410-49514410 |
skin | malignant_melanoma | Substitution - coding silent |
c.321delA; p.G109fs*27; 19:49514129-49514129 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.396G>C; p.K132N; 19:49514281-49514281 |
prostate | carcinoma | Substitution - Missense |
c.916G>A; p.G306S; 19:49525501-49525501 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.295C>T; p.L99L; 19:49514103-49514103 |
breast | carcinoma | Substitution - coding silent |
c.837C>T; p.H279H; 19:49524742-49524742 |
thyroid | other; neoplasm | Substitution - coding silent |
c.125C>T; p.P42L; 19:49513933-49513933 |
oesophagus; upper_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.55C>T; p.P19S; 19:49513455-49513455 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.680A>G; p.Y227C; 19:49524585-49524585 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.129G>T; p.G43G; 19:49513937-49513937 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.316G>C; p.G106R; 19:49514124-49514124 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1060G>A; p.D354N; 19:49526081-49526081 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.616C>T; p.R206C; 19:49524521-49524521 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.849G>A; p.A283A; 19:49524754-49524754 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.724G>A; p.A242T; 19:49524629-49524629 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.315delG; p.G107fs*29; 19:49514123-49514123 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.487C>T; p.R163W; 19:49514372-49514372 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.591G>A; p.L197L; 19:49514476-49514476 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.555C>T; p.R185R; 19:49514440-49514440 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.640C>T; p.P214S; 19:49524545-49524545 |
skin | malignant_melanoma | Substitution - Missense |
c.502G>A; p.D168N; 19:49514387-49514387 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.582C>T; p.R194R; 19:49514467-49514467 |
breast | carcinoma | Substitution - coding silent |
c.582C>T; p.R194R; 19:49514467-49514467 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.356G>T; p.C119F; 19:49514241-49514241 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.466G>A; p.E156K; 19:49514351-49514351 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.739G>A; p.G247S; 19:49524644-49524644 |
skin | malignant_melanoma | Substitution - Missense |
c.890C>T; p.S297F; 19:49525475-49525475 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.370G>A; p.D124N; 19:49514255-49514255 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.892G>A; p.V298M; 19:49525477-49525477 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.85T>A; p.S29T; 19:49513893-49513893 |
breast | carcinoma | Substitution - Missense |
c.75A>C; p.E25D; 19:49513883-49513883 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.762C>T; p.D254D; 19:49524667-49524667 |
pancreas | carcinoma | Substitution - coding silent |
c.693G>A; p.L231L; 19:49524598-49524598 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1068G>T; p.K356N; 19:49526089-49526089 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1068G>T; p.K356N; 19:49526089-49526089 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1068G>T; p.K356N; 19:49526089-49526089 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.547C>T; p.P183S; 19:49514432-49514432 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.248A>G; p.Y83C; 19:49514056-49514056 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.84C>T; p.L28L; 19:49513892-49513892 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.513C>T; p.A171A; 19:49514398-49514398 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.180C>G; p.S60R; 19:49513988-49513988 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.76A>G; p.S26G; 19:49513884-49513884 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.321A>G; p.G107G; 19:49514129-49514129 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.243C>A; p.S81S; 19:49514051-49514051 |
liver | carcinoma | Substitution - coding silent |
c.243C>A; p.S81S; 19:49514051-49514051 |
liver | carcinoma | Substitution - coding silent |
c.938C>T; p.A313V; 19:49525523-49525523 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.193C>T; p.R65W; 19:49514001-49514001 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.118C>G; p.P40A; 19:49513926-49513926 |
thyroid | carcinoma | Substitution - Missense |
c.118C>G; p.P40A; 19:49513926-49513926 |
thyroid | carcinoma | Substitution - Missense |
c.782C>T; p.S261L; 19:49524687-49524687 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.782C>T; p.S261L; 19:49524687-49524687 |
skin | malignant_melanoma | Substitution - Missense |
c.1006C>T; p.R336C; 19:49526027-49526027 |
skin | malignant_melanoma | Substitution - Missense |
c.783G>A; p.S261S; 19:49524688-49524688 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.877C>G; p.P293A; 19:49525462-49525462 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.314_315insG; p.G109fs*12; 19:49514122-49514123 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.617G>A; p.R206H; 19:49524522-49524522 |
breast | carcinoma | Substitution - Missense |