FLT3 (fms related receptor tyrosine kinase 3)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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2322 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Fms related receptor tyrosine kinase 3 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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FLT3 |
SynonymsGene synonyms aliases
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CD135, FLK-2, FLK2, STK1 |
ChromosomeChromosome number
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13 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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13q12.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a class III receptor tyrosine kinase that regulates hematopoiesis. This receptor is activated by binding of the fms-related tyrosine kinase 3 ligand to the extracellular domain, which induces homodimer formation in the plasma membrane le |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs121909646 |
T>A,G |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
rs121913232 |
G>C |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
rs121913486 |
ATC>- |
Pathogenic-likely-pathogenic |
Inframe deletion, non coding transcript variant, coding sequence variant |
rs121913487 |
A>C,T |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
rs121913488 |
C>A,G,T |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
rs121913490 |
GAT>- |
Likely-pathogenic |
Inframe deletion, non coding transcript variant, coding sequence variant |
rs121913491 |
T>C |
Likely-pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
rs376588714 |
T>C |
Likely-pathogenic |
Coding sequence variant, non coding transcript variant, missense variant |
rs398122514 |
->TCCGGA |
Pathogenic |
Coding sequence variant, non coding transcript variant, inframe insertion |
rs587776834 |
TCA>- |
Pathogenic |
Non coding transcript variant, inframe deletion, coding sequence variant |
rs749281035 |
G>A,T |
Likely-pathogenic |
Non coding transcript variant, synonymous variant, missense variant, coding sequence variant |
rs772061268 |
T>G |
Likely-pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
rs864321619 |
->CATATTCTCTGAAATCAACGT |
Pathogenic |
Inframe insertion, coding sequence variant, non coding transcript variant |
rs991132188 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519726 |
T>A,C,G |
Pathogenic, likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519762 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519763 |
TC>AA |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519764 |
A>C,T |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519765 |
T>A,C |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519766 |
G>C,T |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519767 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519768 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057519769 |
C>A |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057520021 |
A>C,G |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057520022 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057520023 |
A>C |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057520024 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057520025 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057520026 |
T>G |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1057520043 |
A>C |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1208575764 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
rs1555256794 |
G>- |
Drug-response |
5 prime UTR variant, frameshift variant, coding sequence variant, non coding transcript variant |
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miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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Transcription factor |
Regulation |
Reference |
PML |
Activation |
17124055 |
STAT3 |
Activation |
16418395 |
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
P36888 |
Protein name |
Receptor-type tyrosine-protein kinase FLT3 (EC 2.7.10.1) (FL cytokine receptor) (Fetal liver kinase-2) (FLK-2) (Fms-like tyrosine kinase 3) (FLT-3) (Stem cell tyrosine kinase 1) (STK-1) (CD antigen CD135) |
Protein function |
Tyrosine-protein kinase that acts as a cell-surface receptor for the cytokine FLT3LG and regulates differentiation, proliferation and survival of hematopoietic progenitor cells and of dendritic cells. Promotes phosphorylation of SHC1 and AKT1, a |
PDB |
1RJB
,
3QS7
,
3QS9
,
4RT7
,
4XUF
,
5X02
,
6IL3
,
6JQR
,
7QDP
,
7ZV9
,
8XB1
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00047 |
ig |
255 → 345 |
Immunoglobulin domain |
Domain |
PF07714 |
PK_Tyr_Ser-Thr |
610 → 943 |
Protein tyrosine and serine/threonine kinase |
Domain |
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Sequence |
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Sequence length |
993 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Autoimmune diseases |
Autoimmune Diseases, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 |
rs41285370, rs869025224 |
30595370 |
Burkitt`s lymphoma |
Burkitt Lymphoma |
rs28933407, rs121918683, rs121918684 |
16234090 |
Hypothyroidism |
Hypothyroidism |
rs869320723, rs121908862, rs121908863, rs121908865, rs121908866, rs121908867, rs121908870, rs121908871, rs121908872, rs2140110277, rs121908881, rs121908884, rs121908885, rs786205080, rs1586182912, rs121917847, rs104893655, rs104893657, rs104893658, rs104893659, rs104893660, rs104893656, rs121917719, rs786204790, rs189261858, rs879255608, rs868197660, rs879255609, rs1586744173, rs1586182837, rs771222349, rs1587618417, rs1601844140, rs760832986, rs780982673, rs1603336347, rs1691155605 |
30595370 |
Lymphoblastic leukemia |
Childhood Acute Lymphoblastic Leukemia, L2 Acute Lymphoblastic Leukemia, Precursor B-cell lymphoblastic leukemia, Precursor B-cell acute lymphoblastic leukemia, Precursor T-Cell Lymphoblastic Leukemia-Lymphoma, Precursor Cell Lymphoblastic Leukemia Lymphoma, Precursor T-cell acute lymphoblastic leukemia |
rs387906351, rs104894562, rs398122513, rs398122840, rs398123063, rs1057524466, rs1064796115, rs1064795660, rs1064793129, rs1064796227, rs1567887558, rs1161194345, rs1597558200, rs1406320425, rs1597566470, rs1597566699, rs1597567692, rs1597567985, rs1438890364, rs1288977950, rs1597552140, rs1597566356, rs1597566726, rs1597568117, rs2069719445, rs2069729948, rs2070018439, rs745708044, rs1169577591 |
16234090 |
Leukemia |
Leukemia, Myelocytic, Acute, Acute Myeloid Leukemia (AML-M2) |
rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297, rs11978267, rs4132601 |
25053825, 19822134, 14604974, 23906301, 23878140, 25157968, 17047150, 22504183, 23036488, 16091740, 11290608, 22368270, 19657110, 19840437, 21928377, 24526162, 24619500, 16990784, 14737077, 15667533, 17606455, 22504185, 20733134, 27992414, 22504184, 16573742, 27099147, 15256420, 23430109, 21482694, 23321257, 23783394, 23261068, 16857985, 15374878, 17184839, 17050201, 16410449, 22504186, 22409268, 15625552, 23714533, 17889720, 21441929, 15863200, 16371029, 24046014, 24526162, 27992414, 25053825, 17184839, 27099147, 23906301, 22409268, 21928377, 23036488, 17050201, 22338050, 21482694, 21441929, 19822134 |
Myelomonocytic leukemia |
Acute myelomonocytic leukemia |
rs137854555, rs267606602, rs267606604, rs137854562, rs267606607, rs121918546, rs112445441, rs121913529, rs121913530, rs121918465, rs267606708, rs267606706, rs121434596, rs121913237, rs397514641, rs199474747, rs199474728, rs199474781, rs587781807, rs727504426, rs786203950, rs786202782, rs1321848637, rs786202457, rs786204157, rs267606599, rs1555535032, rs864622161, rs878853865, rs199474737, rs199474742, rs1057518904, rs771820789, rs1057518974, rs1057518807, rs1057521098, rs1057521848, rs1060500273, rs376576925, rs1060500356, rs1060500363, rs1060500245, rs1060500387, rs1064794278, rs1085307819, rs753245823, rs1135402868, rs1135402894, rs1555610893, rs1555610881, rs771115661, rs1555614453, rs753529924, rs1555618572, rs1555534697, rs1555610905, rs1555613543, rs1131691105, rs1555534893, rs1060500376, rs1060500355, rs1567845945, rs1567817974, rs1567818033, rs1597713360, rs1555614462, rs137854553, rs1597831990, rs1597858459, rs1597858594, rs876657932, rs1597681200, rs1597866846, rs1597710409, rs2066138676, rs2066507116, rs2066874267, rs2066874810, rs1555614354, rs786202177, rs2069448326, rs2069793099, rs863224445 |
23783394 |
Tourette syndrome |
Gilles de la Tourette syndrome |
rs193302861, rs191284403, rs267606861 |
30818990 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Csf pleocytosis |
Pleocytosis |
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27725143, 27099147 |
Erythroleukemia |
Acute erythroleukemia, Acute erythroleukemia - M6a subtype, Acute erythroleukemia - M6b subtype |
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30926971 |
Lymphocytic leukemia |
Acute lymphocytic leukemia |
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Mixed phenotype leukemia |
Mixed phenotype acute leukemia |
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29072953, 26276768, 27069254 |
Myeloblastic leukemia with maturation |
Acute myeloblastic leukemia with maturation |
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Myeloblastic leukemia without maturation |
Acute myeloblastic leukemia without maturation |
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Myeloid leukemia |
Acute Myeloid Leukemia, M1, Acute myeloid leukemia, minimal differentiation, Acute myeloid leukemia FAB-M6, Acute myeloid leukemia with minimal differentiation |
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23906301, 27099147, 25053825, 17050201, 21482694, 27992414, 22338050, 21441929, 24526162, 19822134, 17184839, 22409268, 21928377, 23036488, 22338050, 30926971 |
Myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) |
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) |
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Myeloid leukemia with t(8;21)(q22;q22) translocation |
Acute myeloid leukemia with t(8;21)(q22;q22) translocation |
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Promyelocytic leukemia |
Acute Promyelocytic Leukemia |
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26285909, 24160850, 17454189 |
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