TSC1
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Homo sapiens |
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TSC1 is differentially expressed in 216 experiments: 102 organism parts: lung, bone marrow, ... (100 more);, 144 disease states: normal, glioblastoma, ... (142 more);, 54 cell types 294 cell lines 25 compound treatments and 59 other conditions. |
| Synonyms |
hamartin, TSC, LAM, KIAA0243 |
| Orthologs |
Tsc1
(Rattus norvegicus)
TSC1
(Gallus gallus)
Tsc1
(Mus musculus)
tsc1b
(Danio rerio)
A6QQZ6_BOVIN
(Bos taurus)
ENSCING00000004555
(Ciona intestinalis)
tsc1a
(Danio rerio)
Tsc1
(Drosophila melanogaster)
tsc1
(Xenopus laevis)
tsc1
(Xenopus laevis)
TSC1
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
cytosol, embryo development, protein stabilization, protein binding, cardiac muscle cell differentiation, actin filament, cytoplasm, cell cortex, regulation of cell-matrix adhesion, negative regulation of cell proliferation, protein complex, membrane, protein N-terminus binding, chaperone binding, cell cycle arrest, regulation of translation, regulation of protein kinase activity, insulin receptor signaling pathway, potassium ion transport, membrane fraction, regulation of phosphoprotein phosphatase activity, synapse organization, microsome, cell-matrix adhesion, activation of Rho GTPase activity, lamellipodium, negative regulation of TOR signaling cascade, growth cone, nervous system development, regulation of actin cytoskeleton organization, cell projection organization, negative regulation of translation, GTPase activating protein binding, negative regulation of cell size, TSC1-TSC2 complex, positive regulation of focal adhesion assembly, myelination, neural tube closure, kidney development, cerebral cortex development, regulation of focal adhesion assembly, GTPase regulator activity, cytoskeletal part, response to insulin stimulus, hippocampus development, regulation of stress fiber assembly, rRNA export from nucleus, protein heterooligomerization |
| Gene Ontology ID |
GO:0008286, GO:0008285, GO:0016020, GO:0007050, GO:0007160, GO:0009790, GO:0007399, GO:0005938, GO:0051087, GO:0030426, GO:0005624, GO:0005515, GO:0047485, GO:0005737, GO:0043666, GO:0005884, GO:0005829, GO:0005792, GO:0006813, GO:0055007, GO:0001952, GO:0006417, GO:0050808, GO:0050821, GO:0032794, GO:0032862, GO:0045792, GO:0032956, GO:0043234, GO:0045859, GO:0030030, GO:0030027, GO:0032007, GO:0017148, GO:0051291, GO:0030695, GO:0042552, GO:0006407, GO:0032868, GO:0044430, GO:0051894, GO:0051893, GO:0001822, GO:0001843, GO:0051492, GO:0021987, GO:0021766, GO:0033596 |
| Ensembl Family Description |
HAMARTIN TUBEROUS SCLEROSIS 1 |
| Ensembl Family |
ENSFM00250000002956 |
| InterPro Term |
Hamartin |
| InterPro ID |
IPR007483 |
| Description |
tuberous sclerosis 1 [Source:HGNC Symbol;Acc:12362] |
| EMBL-Bank ID |
D87683, AF013168, AF234185, AL445645, AK303030, BC047772, CH471090, AC002096, BC070032, AK299654 |
| UniGene ID |
Hs.370854, Hs.713977 |
| UniProt Accession |
Q92574, Q86WV8, B7Z897, B7Z604, F5H701 |
| HGNC Symbol |
TSC1 |
| Entrez Gene ID |
7248 |
| Ensembl Protein ID |
ENSP00000298552, ENSP00000394524, ENSP00000393473, ENSP00000386093, ENSP00000444017, ENSP00000438099 |
| RefSeq ID |
NP_001155898, NP_001155899, NM_001162426, NM_001162427, NP_000359, NM_000368 |
| Ensembl Gene ID |
ENSG00000165699 |
| Ensembl Transcript ID |
ENST00000493467, ENST00000403810, ENST00000424271, ENST00000475903, ENST00000537172, ENST00000298552, ENST00000490179, ENST00000545250, ENST00000440111, ENST00000461879 |
| Gene-Disease Assocation |
TUBEROUS SCLEROSIS 1; TSC1, FOCAL CORTICAL DYSPLASIA OF TAYLOR; FCDT, LYMPHANGIOLEIOMYOMATOSIS; LAM |
| Design Element |
ENST00000298552, 209390_at, ENST00000461879, ENST00000537172, ENST00000440111, Hs.69429.0.S1_3p_at, ENST00000493467, ENST00000545250, ENST00000424271, D87683_at, g2331280_3p_at, 32599_at, ENST00000475903, ENST00000403810, 55939_at, ENST00000490179 |
| Search EB-eye |
ENSG00000165699
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