gptkbp:instanceOf
|
gptkb:gene
|
gptkbp:alternativeSplicing
|
yes
|
gptkbp:associatedWith
|
nemaline myopathy
cap myopathy
congenital fiber-type disproportion
|
gptkbp:biologicalProcess
|
muscle contraction
structural constituent of muscle
|
gptkbp:cellularComponent
|
thin filament
|
gptkbp:discoveredIn
|
1986
|
gptkbp:encodes
|
tropomyosin alpha-3 chain
|
gptkbp:Entrez_Gene_ID
|
7170
ENSG00000143549
|
gptkbp:expressedIn
|
gptkb:skeletal_muscle
|
gptkbp:fullName
|
tropomyosin 3
|
gptkbp:function
|
regulation of muscle contraction
|
gptkbp:geneType
|
protein-coding
|
gptkbp:hasTranscriptVariant
|
multiple
|
gptkbp:HGNC_ID
|
12013
|
https://www.w3.org/2000/01/rdf-schema#label
|
TPM3
|
gptkbp:interactsWith
|
gptkb:actin
troponin complex
|
gptkbp:length
|
10 exons
|
gptkbp:locatedOnChromosome
|
1q21.2
|
gptkbp:mutationAssociatedWith
|
muscle weakness
|
gptkbp:OMIM
|
191030
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
gptkbp:orthologInMouse
|
Tpm3
|
gptkbp:pathway
|
muscle contraction pathway
|
gptkbp:product
|
tropomyosin alpha-3 chain
|
gptkbp:RefSeq
|
NM_152263
|
gptkbp:UniProtID
|
P06753
|
gptkbp:bfsParent
|
gptkb:ALK_rearrangement
|
gptkbp:bfsLayer
|
5
|