KEGG   Homo sapiens (human): 7125
Entry
7125              CDS       T01001                                 
Symbol
TNNC2, CFAP85, CMYO15, CMYP15, FAP85, MYONRI
Name
(RefSeq) troponin C2, fast skeletal type
  KO
K12042  troponin C, skeletal muscle
Organism
hsa  Homo sapiens (human)
Pathway
hsa04020  Calcium signaling pathway
hsa04814  Motor proteins
hsa04820  Cytoskeleton in muscle cells
Network
nt06539  Cytoskeleton in muscle cells
  Element
N01818  Actin thin filament, muscle contraction
Disease
H01810  Congenital myopathy
Drug target
Reldesemtiv: D11363
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    7125 (TNNC2)
 09140 Cellular Processes
  09142 Cell motility
   04814 Motor proteins
    7125 (TNNC2)
   04820 Cytoskeleton in muscle cells
    7125 (TNNC2)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04812 Cytoskeleton proteins [BR:hsa04812]
    7125 (TNNC2)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Actin filaments / Microfilaments
   Actin-binding proteins
    Troponins
     7125 (TNNC2)
SSDB
Motif
Pfam: EF-hand_7 EF-hand_1 EF-hand_6 EF-hand_8 EF-hand_5 EF-hand_9 AIF-1 EH SPARC_Ca_bdg TerB EF_EFCAB10_C DUF1456 DUF5580_M p25-alpha SurA_N_3 DUF533 CDI_toxin_EC869_like
Other DBs
NCBI-GeneID: 7125
NCBI-ProteinID: NP_003270
OMIM: 191039
HGNC: 11944
Ensembl: ENSG00000101470
UniProt: P02585
Structure
LinkDB
Position
20:complement(45823214..45833306)
AA seq 160 aa
MTDQQAEARSYLSEEMIAEFKAAFDMFDADGGGDISVKELGTVMRMLGQTPTKEELDAII
EEVDEDGSGTIDFEEFLVMMVRQMKEDAKGKSEEELAECFRIFDRNADGYIDPEELAEIF
RASGEHVTDEEIESLMKDGDKNNDGRIDFDEFLKMMEGVQ
NT seq 483 nt   +upstreamnt  +downstreamnt
atgacggaccagcaggctgaggccaggtcctacctcagcgaagagatgatcgctgagttc
aaggctgcctttgacatgtttgatgctgatggtggtggggacatcagcgtcaaggagttg
ggcacggtgatgaggatgctgggccagacacccaccaaggaggagctggacgccatcatc
gaggaggtggatgaggacggcagcggcaccatcgacttcgaggagttcttggtcatgatg
gtgcgccagatgaaagaggacgcgaaagggaagagcgaggaggagctggccgagtgcttc
cgcatcttcgacaggaatgcagacggctacatcgacccggaggagctggctgagattttc
agggcctccggggagcacgtgacggacgaggagatcgaatctctgatgaaagacggcgac
aagaacaacgacggccgcattgacttcgacgagttcctgaagatgatggagggcgtgcag
taa

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