Gene Gene information from NCBI Gene database.
Entrez ID 340156
Gene name Myosin light chain kinase family member 4
Gene symbol MYLK4
Synonyms (NCBI Gene)
SgK085
Chromosome 6
Chromosome location 6p25.2
miRNA miRNA information provided by mirtarbase database.
187
miRTarBase ID miRNA Experiments Reference
MIRT656057 hsa-miR-6871-3p HITS-CLIP 23824327
MIRT656056 hsa-miR-1197 HITS-CLIP 23824327
MIRT656055 hsa-miR-5586-5p HITS-CLIP 23824327
MIRT656054 hsa-miR-3065-3p HITS-CLIP 23824327
MIRT656053 hsa-miR-4530 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0004672 Function Protein kinase activity IEA
GO:0004674 Function Protein serine/threonine kinase activity IEA
GO:0004687 Function Myosin light chain kinase activity IBA
GO:0005515 Function Protein binding IPI 22939624, 28514442, 32707033, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86YV6
Protein name Myosin light chain kinase family member 4 (EC 2.7.11.1) (Sugen kinase 85) (SgK085)
PDB 2X4F
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 106 361 Protein kinase domain Domain
Sequence
Sequence length 388
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Calcium signaling pathway
cGMP-PKG signaling pathway
Vascular smooth muscle contraction
Apelin signaling pathway
Focal adhesion
Platelet activation
Regulation of actin cytoskeleton
Oxytocin signaling pathway
Gastric acid secretion
 
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Long QT syndrome Likely benign rs796052168 RCV000190165
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Cardiomyopathies Associate 24709777
Cardiomyopathy Dilated Inhibit 24709777