KEGG   ORTHOLOGY: K10354Help
Entry
K10354                      KO                                     

Name
ACTA1
Definition
actin, alpha skeletal muscle
Disease
H00698  
Nemaline myopathy
H00701  
Congenital fiber type disproportion (CFTD)
H00702  
Cap myopathy
Brite
Cytoskeleton proteins [BR:ko04812]
 Eukaryotic cytoskeleton proteins
  Actin filaments / Microfilaments
   Actins
    Actins
     K10354  ACTA1; actin, alpha skeletal muscle
BRITE hierarchy
Genes
HSA: 
58(ACTA1)
PTR: 
100609865(ACTA1)
PPS: 
100987270(ACTA1)
GGO: 
101154134(ACTA1)
PON: 
100172818(ACTA1)
NLE: 
100589549(ACTA1)
MCC: 
100426612(ACTA1)
MCF: 
102121165(ACTA1)
RRO: 
104670692(ACTA1)
CJC: 
100395910(ACTA1)
MMU: 
11459(Acta1)
RNO: 
29437(Acta1)
CGE: 
100768972(Acta1)
NGI: 
103744113(Acta1)
HGL: 
101721383(Acta1)
OCU: 
100009506(ACTA1)
TUP: 
102487372(ACTA1)
CFA: 
488984(ACTA1)
AML: 
100473191(ACTA1)
UMR: 
103661861(ACTA1)
FCA: 
101095439(ACTA1)
BTA: 
281592(ACTA1)
BOM: 
102271625(ACTA1)
PHD: 
102330461(ACTA1)
CHX: 
102182476(ACTA1)
OAS: 
101107662(ACTA1)
SSC: 
100154254(ACTA1)
CFR: 
102507445(ACTA1)
BACU: 
103000661(ACTA1)
LVE: 
103078221(ACTA1)
ECB: 
100065454(ACTA1)
PALE: 
102891483(ACTA1)
MDO: 
SHR: 
OAA: 
GGA: 
421534(ACTA1)
MGP: 
100542212(ACTA1)
APLA: 
101802755(ACTA1)
TGU: 
100231853(ACTA1)
GFR: 
102037155(ACTA1)
FAB: 
101817592(ACTA1)
PHI: 
102100709(ACTA1)
CCW: 
104684304(ACTA1)
FPG: 
101916472(ACTA1)
FCH: 
102059001(ACTA1)
CLV: 
102087353(ACTA1)
ASN: 
102384256(ACTA1) 102388669(ACTRT3)
AMJ: 
102562188(ACTRT3) 102576327(ACTA1)
PSS: 
CMY: 
102943964(ACTA1)
ACS: 
100566789(acta1)
PBI: 
103051164(ACTA1)
XLA: 
379351(MGC53823) 398426(act3)
DRE: 
407658(acta1b)
TRU: 
LCM: 
BFO: 
CIN: 
 » show all
TaxonomyKoalaUniProt
Reference
  Authors
Lindqvist J, Cheng AJ, Renaud G, Hardeman EC, Ochala J
  Title
Distinct underlying mechanisms of limb and respiratory muscle fiber weaknesses in nemaline myopathy.
  Journal
J Neuropathol Exp Neurol 72:472-81 (2013)
  Sequence
[hsa:58]

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