Protein Tsc1

URN urn:agi-llid:7248
Total Entities 0
Connectivity 610
Name Tsc1
Description tuberous sclerosis 1
Notes This gene encodes a growth inhibitory protein thought to play a role in the stabilization of tuberin. Mutations in this gene have been associated with tuberous sclerosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq]

GO Molecular Function GTPase regulator activity
chaperone binding
protein N-terminus binding
GTPase activating protein binding

GO Cellular Component membrane
actin filament
protein complex
TSC1-TSC2 complex
cytoplasm
cell cortex
cytosol
intracellular membrane-bounded organelle
cytoskeleton
growth cone
lamellipodium

GO Biological Process activation of Rho GTPase activity
myelination
embryo development
nervous system development
kidney development
cardiac muscle cell differentiation
cerebral cortex development
hippocampus development
neural tube closure
cell projection organization
synapse organization
regulation of actin cytoskeleton organization
regulation of stress fiber assembly
cell cycle arrest
negative regulation of TOR signaling
insulin receptor signaling pathway
regulation of cell-matrix adhesion
regulation of focal adhesion assembly
positive regulation of focal adhesion assembly
cell-matrix adhesion
negative regulation of cell size
negative regulation of cell proliferation
rRNA export from nucleus
potassium ion transport
response to insulin
negative regulation of translation
regulation of translation
regulation of protein kinase activity
regulation of phosphoprotein phosphatase activity
protein stabilization
protein heterooligomerization

Pathway Insulin Influence on Protein Synthesis
Proteins Involved in Pathogenesis of Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome Overview
Proteins Involved in Pathogenesis of Epilepsy
Epilepsies Associated with Blood-Brain Barrier Disruption
mTOR Hyperactivation after Status Epilepticus
Proposed Mechanisms of Antiepileptic Effects of a Ketogenic Diet
Preconditioning Ischemia
EGFR/ERBB2 -> HIF1A signaling
AREG/HIF1A Expression Targets
EGF/HIF1A Expression Targets
EREG/HIF1A Expression Target
HBEGF/HIF1A Expression Targets
NRG1/HIF1A Expression Target
TGFA/HIF1A Expression Targets
mTOR signaling pathway
mTOR signaling pathway

Group PSC
GTPase regulator activity
activation of Rho GTPase activity
myelination
embryo development
nervous system development
kidney development
cardiac muscle cell differentiation
cerebral cortex development
hippocampus development
neural tube closure
cell projection organization
synapse organization
regulation of actin cytoskeleton organization
regulation of stress fiber assembly
cell cycle arrest
negative regulation of TOR signaling
insulin receptor signaling pathway
regulation of cell-matrix adhesion
regulation of focal adhesion assembly
positive regulation of focal adhesion assembly
cell-matrix adhesion
negative regulation of cell size
negative regulation of cell proliferation
rRNA export from nucleus
potassium ion transport
response to insulin
negative regulation of translation
regulation of translation
regulation of protein kinase activity
regulation of phosphoprotein phosphatase activity
protein stabilization
protein heterooligomerization
chaperone binding
protein N-terminus binding
GTPase activating protein binding
membrane
actin filament
protein complex
TSC1-TSC2 complex
cytoplasm
cell cortex
cytosol
intracellular membrane-bounded organelle
cytoskeleton
growth cone
lamellipodium
Proteins Involved in Pathogenesis of Cowden Syndrome
Disease Genes Identified in Syndromic Epilepsy
Disease Genes Identified in Epilepsy with Mental Retardation and Brain Malformations
Secreted proteins

LocusLink ID 7248
64930
60445

Cell Localization Cytoplasm
Membrane

GO ID 0032794
0030695
0051087
0047485
0032862
0055007
0007050
0030030
0007160
0021987
0021766
0008286
0001822
0042552
0032007
0008285
0045792
0017148
0001843
0051894
0006813
0051291
0050821
0006407
0001952
0043666
0045859
0051492
0006417
0032868
0050808
0033596
0005884
0005938
0005737
0005829
0030426
0043231
0030027
0016020
0043234
0009790
0007399
0032956
0051893
0005856
0045786
0031397
0005624
0009987
0005515
0007049
0044430
0005792
0007266
0007155
0050875

Alias LAM
TSC
hamartin
tumor suppressor
tuberous sclerosis 1 protein
mKIAA0243
RP23-362N19.3
tuberous sclerosis 1 protein homolog
Kiaa0243
TSC I
TSC1
TSC1 gene (hamartin)
tuberous sclerosis I
tuberous sclerosis 1
MGC86987
tuberous sclerosis 1 (hamartin)
OTTMUSP00000012523
OTTHUMP00000022439
OTTHUMP00000198378
OTTMUSP00000012518
OTTMUSP00000012519
OTTMUSP00000012522

Mouse chromosome position 2
2 B-C1.1

OMIM ID 605284
607341
606690
191100

Rat chromosome position 3p12

Hugo ID 12362

Human chromosome position 9q34

Swiss-Prot Accession Q86WV8
Q92574
Q32NF0
Q9EP53
Q9Z136
B7Z897
Q5VVN5
A2AHW1
Q3UHF2
Q7TS92
Q80U55
Q924U7
Q96RT4
Q59IT9
Q8BQP0
Q96RT3
Q0VAM5

PIR ID T03814

GenBank ID NC_000009
NM_001162427
NP_001155899
NM_001162426
NP_001155898
NM_000368
NP_000359
XM_005272211
XP_005272268
XM_005272212
XP_005272269
NG_012386
NC_018920
AC_000141
ABBA01032478
ABBA01032479
AF234185
AAF61948
AF274228
AAK60415
AF274229
AAK60416
AL445645
AMYH02021817
AMYH02021818
AMYH02021819
CH471090
EAW88021
AA215977
AB190910
BAD91314
AF013168
AAC51674
AK297326
BAH12548
AK299654
BAH13090
AK303030
BAH13883
AK308412
BC047772
AAH47772
BC070032
AAH70032
BC108668
AAI08669
BC121000
AAI21001
BI463204
D87683
BAA13436
DA726552
N63914
Q92574
BC167824
AAI67824
NC_000068
XM_006498221
XP_006498284
XM_006498224
XP_006498287
XM_006498220
XP_006498283
XM_006498223
XP_006498286
XM_006498225
XP_006498288
NM_022887
NP_075025
XM_006498222
XP_006498285
AC_000024
AAHY01014899
AJ271911
CAC20676
AL731851
CH466542
EDL08392
AB047561
BAB60810
AJ271912
CAC20677
AK030318
AK047656
BAC33114
AK078140
AK083363
AK122229
BAC65511
AK147428
BAE27905
AK154416
BC052399
AAH52399
Q9EP53
NC_005102
XM_006233849
XP_006233911
XM_006233843
XP_006233905
XM_006233844
XP_006233906
XM_006233845
XP_006233907
XM_006233847
XP_006233909
XM_006233848
XP_006233910
XM_006233846
XP_006233908
NM_021854
NP_068626
AC_000071
AABR06022089
AAHX01020594
CH474001
EDL93403
AB011821
BAA75254
AB016165
BAA75255
Q9Z136
NM_001008567
NP_001008567
NT_035014
NW_924573
NW_001839241
AC_000052
CAH72112
CR622174
Q0VAM5
Q32NF0
Q59IT9
Q5VVN5
Q86WV8
Q96RT3
Q96RT4
NT_039206
NW_001030686
CAM22294
CAM22295
Q3UHF2
Q7TS92
Q80U55
Q8BQP0
Q924U7
NW_001084810
NW_047651
BG073522
NW_000174
CAM22296

Unigene ID Hs.370854
Mm.224354
Rn.205837
Rn.230448
Rn.15894

KEGG ID hsa:7248
mmu:64930
rno:60445

Swiss-Prot ID TSC1_RAT
TSC1_HUMAN
TSC1_MOUSE
Q86WV8_HUMAN
B7Z897_HUMAN
Q32NF0_HUMAN
Q5VVN5_HUMAN
Q3UHF2_MOUSE
Q924U7_MOUSE

Ensembl ID ENSG00000165699
ENSP00000298552
ENST00000298552
ENSP00000444017
ENST00000545250
ENSP00000394524
ENST00000440111
ENSMUSG00000026812
ENSMUSP00000109501
ENSMUST00000113870
ENSMUSP00000028155
ENSMUST00000028155
ENSMUSP00000109498
ENSMUST00000113867
ENSRNOG00000011470
ENSRNOP00000016904
ENSRNOT00000016904

Homologene ID 314

Organism Homo sapiens
Mus musculus
Rattus norvegicus

MGI ID 1929183

RGD ID 620124

MedScan ID 7248

IPI ID IPI00109178
IPI00754969
IPI00756571
IPI00943454
IPI00022043
IPI00208147
IPI00384490
IPI00921907
IPI00936896
IPI00745368
IPI00894971
IPI00895026