Homo sapiens (human): 7168
Help
Entry
7168 CDS
T01001
Symbol
TPM1, C15orf13, CMD1Y, CMH3, HEL-S-265, HTM-alpha, LVNC9, TMSA
Name
(RefSeq) tropomyosin 1
KO
K10373
tropomyosin 1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04260
Cardiac muscle contraction
hsa04261
Adrenergic signaling in cardiomyocytes
hsa04814
Motor proteins
hsa04820
Cytoskeleton in muscle cells
hsa05206
MicroRNAs in cancer
hsa05410
Hypertrophic cardiomyopathy
hsa05414
Dilated cardiomyopathy
Network
nt06539
Cytoskeleton in muscle cells
Element
N01818
Actin thin filament, muscle contraction
N01819
Actin thin filament, length regulation
Disease
H00292
Hypertrophic cardiomyopathy
H00294
Dilated cardiomyopathy
H01216
Left ventricular noncompaction
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04814 Motor proteins
7168 (TPM1)
04820 Cytoskeleton in muscle cells
7168 (TPM1)
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
7168 (TPM1)
04261 Adrenergic signaling in cardiomyocytes
7168 (TPM1)
09160 Human Diseases
09161 Cancer: overview
05206 MicroRNAs in cancer
7168 (TPM1)
09166 Cardiovascular disease
05410 Hypertrophic cardiomyopathy
7168 (TPM1)
05414 Dilated cardiomyopathy
7168 (TPM1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
7168 (TPM1)
04147 Exosome [BR:
hsa04147
]
7168 (TPM1)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Actin filaments / Microfilaments
Actin-binding proteins
Tropomyosins
7168 (TPM1)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of microglial cells
7168 (TPM1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Tropomyosin
CLZ
Laminin_II
TMF_DNA_bd
ERM_helical
NBP1
ATG16
CENP-F_leu_zip
DUF745
XhlA
Laminin_I
Crescentin
Motif
Other DBs
NCBI-GeneID:
7168
NCBI-ProteinID:
NP_000357
OMIM:
191010
HGNC:
12010
Ensembl:
ENSG00000140416
UniProt:
P09493
A0A0K0K1I0
Structure
PDB
LinkDB
All DBs
Position
15:63042747..63071915
Genome browser
AA seq
284 aa
AA seq
DB search
MDAIKKKMQMLKLDKENALDRAEQAEADKKAAEDRSKQLEDELVSLQKKLKGTEDELDKY
SEALKDAQEKLELAEKKATDAEADVASLNRRIQLVEEELDRAQERLATALQKLEEAEKAA
DESERGMKVIESRAQKDEEKMEIQEIQLKEAKHIAEDADRKYEEVARKLVIIESDLERAE
ERAELSEGQVRQLEEQLRIMDQTLKALMAAEDKYSQKEDRYEEEIKVLSDKLKEAETRAE
FAERSVTKLEKSIDDLEDELYAQKLKYKAISEELDHALNDMTSM
NT seq
855 nt
NT seq
+upstream
nt +downstream
nt
atggacgccatcaagaagaagatgcagatgctgaagctcgacaaggagaacgccttggat
cgagctgagcaggcggaggccgacaagaaggcggcggaagacaggagcaagcagctggaa
gatgagctggtgtcactgcaaaagaaactcaagggcaccgaagatgaactggacaaatac
tctgaggctctcaaagatgcccaggagaagctggagctggcagagaaaaaggccaccgat
gctgaagccgacgtagcttctctgaacagacgcatccagctggttgaggaagagttggat
cgtgcccaggagcgtctggcaacagctttgcagaagctggaggaagctgagaaggcagca
gatgagagtgagagaggcatgaaagtcattgagagtcgagcccaaaaagatgaagaaaaa
atggaaattcaggagatccaactgaaagaggccaagcacattgctgaagatgccgaccgc
aaatatgaagaggtggcccgtaagctggtcatcattgagagcgacctggaacgtgcagag
gagcgggctgagctctcagaaggccaagtccgacagctggaagaacaattaagaataatg
gatcagaccttgaaagcattaatggctgcagaggataagtactcgcagaaggaagacaga
tatgaggaagagatcaaggtcctttccgacaagctgaaggaggctgagactcgggctgag
tttgcggagaggtcagtaactaaattggagaaaagcattgatgacttagaagacgagctg
tacgctcagaaactgaagtacaaagccatcagcgaggagctggaccacgctctcaacgat
atgacttccatgtaa
Homo sapiens (human): 7169
Help
Entry
7169 CDS
T01001
Symbol
TPM2, AMCD1, CMYP23, DA1, DA2B, DA2B4, HEL-S-273, NEM4, TMSB
Name
(RefSeq) tropomyosin 2
KO
K10374
tropomyosin 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04260
Cardiac muscle contraction
hsa04261
Adrenergic signaling in cardiomyocytes
hsa04814
Motor proteins
hsa04820
Cytoskeleton in muscle cells
hsa05410
Hypertrophic cardiomyopathy
hsa05414
Dilated cardiomyopathy
Network
nt06539
Cytoskeleton in muscle cells
Element
N01818
Actin thin filament, muscle contraction
N01819
Actin thin filament, length regulation
Disease
H00698
Nemaline myopathy
H00702
Cap myopathy
H00811
Distal arthrogryposis
H01810
Congenital myopathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04814 Motor proteins
7169 (TPM2)
04820 Cytoskeleton in muscle cells
7169 (TPM2)
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
7169 (TPM2)
04261 Adrenergic signaling in cardiomyocytes
7169 (TPM2)
09160 Human Diseases
09166 Cardiovascular disease
05410 Hypertrophic cardiomyopathy
7169 (TPM2)
05414 Dilated cardiomyopathy
7169 (TPM2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
7169 (TPM2)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Actin filaments / Microfilaments
Actin-binding proteins
Tropomyosins
7169 (TPM2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Tropomyosin
CLZ
Laminin_II
ERM_helical
CENP-F_leu_zip
TMF_DNA_bd
Snapin_Pallidin
Crescentin
YscO
Lebercilin
SlyX
MscS_porin
ATG16
Suppressor_APC
DUF16
CCDC93_CC
DUF1664
Fez1
Motif
Other DBs
NCBI-GeneID:
7169
NCBI-ProteinID:
NP_003280
OMIM:
190990
HGNC:
12011
Ensembl:
ENSG00000198467
UniProt:
P07951
LinkDB
All DBs
Position
9:complement(35681993..35690056)
Genome browser
AA seq
284 aa
AA seq
DB search
MDAIKKKMQMLKLDKENAIDRAEQAEADKKQAEDRCKQLEEEQQALQKKLKGTEDEVEKY
SESVKEAQEKLEQAEKKATDAEADVASLNRRIQLVEEELDRAQERLATALQKLEEAEKAA
DESERGMKVIENRAMKDEEKMELQEMQLKEAKHIAEDSDRKYEEVARKLVILEGELERSE
ERAEVAESKCGDLEEELKIVTNNLKSLEAQADKYSTKEDKYEEEIKLLEEKLKEAETRAE
FAERSVAKLEKTIDDLEDEVYAQKMKYKAISEELDNALNDITSL
NT seq
855 nt
NT seq
+upstream
nt +downstream
nt
atggacgccatcaagaagaagatgcagatgctgaagctggacaaggagaacgccatcgac
cgcgccgagcaggccgaagccgacaagaagcaagctgaggaccgctgcaagcagctggag
gaggagcagcaggccctccagaagaagctgaaggggacagaggatgaggtggaaaagtat
tctgaatccgtgaaggaggcccaggagaaactggagcaggccgagaagaaggccactgat
gctgaggcagatgtggcctccctgaaccgccgcattcagctggttgaggaggagctggac
cgggcccaggagcgcctggctacagccctgcagaagctggaggaggccgagaaggcggct
gatgagagcgagagaggaatgaaggtcatcgaaaaccgggccatgaaggatgaggagaag
atggaactgcaggagatgcagctgaaggaggccaagcacatcgctgaggattcagaccgc
aaatatgaagaggtggccaggaagctggtgatcctggaaggagagctggagcgctcggag
gagagggctgaggtggccgagagtaaatgtggggacctagaggaggagctgaaaattgtt
accaacaacttgaaatccctggaggcccaggcggacaagtattccaccaaagaagataaa
tatgaagaggagatcaaactgttggaggagaagctgaaggaggctgagacccgagcagag
tttgccgagaggtctgtggcaaagttggagaaaaccatcgatgacctagaagatgaagtc
tatgcccagaagatgaagtacaaggccattagcgaggaactggacaacgcactcaatgac
atcacctccctctga
Homo sapiens (human): 7170
Help
Entry
7170 CDS
T01001
Symbol
TPM3, CAPM1, CFTD, CMYP4A, CMYP4B, HEL-189, HEL-S-82p, NEM1, OK/SW-cl.5, TM-5, TM3, TM30, TM30nm, TM5, TPM3nu, TPMsk3, TRK, hscp30
Name
(RefSeq) tropomyosin 3
KO
K09290
tropomyosin 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa04260
Cardiac muscle contraction
hsa04261
Adrenergic signaling in cardiomyocytes
hsa04814
Motor proteins
hsa04820
Cytoskeleton in muscle cells
hsa05200
Pathways in cancer
hsa05216
Thyroid cancer
hsa05410
Hypertrophic cardiomyopathy
hsa05414
Dilated cardiomyopathy
Network
nt06539
Cytoskeleton in muscle cells
Element
N01818
Actin thin filament, muscle contraction
N01819
Actin thin filament, length regulation
Disease
H00032
Thyroid cancer
H00698
Nemaline myopathy
H00701
Congenital fiber type disproportion
H00702
Cap myopathy
H01810
Congenital myopathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04814 Motor proteins
7170 (TPM3)
04820 Cytoskeleton in muscle cells
7170 (TPM3)
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
7170 (TPM3)
04261 Adrenergic signaling in cardiomyocytes
7170 (TPM3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
7170 (TPM3)
09162 Cancer: specific types
05216 Thyroid cancer
7170 (TPM3)
09166 Cardiovascular disease
05410 Hypertrophic cardiomyopathy
7170 (TPM3)
05414 Dilated cardiomyopathy
7170 (TPM3)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
7170 (TPM3)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Actin filaments / Microfilaments
Actin-binding proteins
Tropomyosins
7170 (TPM3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Tropomyosin
Laminin_II
CLZ
Crescentin
TMF_DNA_bd
DUF745
Lebercilin
ATG16
DUF3450
XhlA
CENP-F_leu_zip
Nuf2_DHR10-like
DUF1664
SlyX
Laminin_I
Motif
Other DBs
NCBI-GeneID:
7170
NCBI-ProteinID:
NP_689476
OMIM:
191030
HGNC:
12012
Ensembl:
ENSG00000143549
UniProt:
P06753
Structure
PDB
LinkDB
All DBs
Position
1:complement(154155308..154192100)
Genome browser
AA seq
285 aa
AA seq
DB search
MMEAIKKKMQMLKLDKENALDRAEQAEAEQKQAEERSKQLEDELAAMQKKLKGTEDELDK
YSEALKDAQEKLELAEKKAADAEAEVASLNRRIQLVEEELDRAQERLATALQKLEEAEKA
ADESERGMKVIENRALKDEEKMELQEIQLKEAKHIAEEADRKYEEVARKLVIIEGDLERT
EERAELAESKCSELEEELKNVTNNLKSLEAQAEKYSQKEDKYEEEIKILTDKLKEAETRA
EFAERSVAKLEKTIDDLEDELYAQKLKYKAISEELDHALNDMTSI
NT seq
858 nt
NT seq
+upstream
nt +downstream
nt
atgatggaggccatcaagaaaaagatgcagatgctgaagttagacaaggagaatgctctg
gatcgggcagagcaagctgaagctgagcagaagcaggcagaagaaagaagtaaacagctg
gaggatgagctggcagccatgcagaagaagctgaaagggacagaggatgagctggacaag
tattctgaagctttgaaggatgcccaggagaagctggaactggcagagaagaaggctgct
gatgctgaggctgaggtggcctccttgaaccgtaggatccagctggttgaagaagagctg
gaccgtgctcaggagcgcctggccactgccctgcaaaagctggaagaagctgaaaaagct
gctgatgagagtgagagaggtatgaaggttattgaaaaccgggccttaaaagatgaagaa
aagatggaactccaggaaatccaactcaaagaagctaagcacattgcagaagaggcagat
aggaagtatgaagaggtggctcgtaagttggtgatcattgaaggagacttggaacgcaca
gaggaacgagctgagctggcagagtctaagtgttctgagctggaggaggagctgaagaat
gtcaccaacaacctcaagtctcttgaggctcaggcggagaagtactctcaaaaagaagat
aaatatgaggaagaaatcaagattcttactgataaactcaaggaggcagagacccgtgct
gagtttgctgagagatcggtagccaagctggaaaagacaattgatgacctggaagatgag
ctctatgcccagaaactgaagtacaaggccattagcgaggagctggaccacgccctcaat
gacatgacctctatataa
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integrated database retrieval system