GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
GO_REF:0000052
Gene Ontology annotation based on curation of immunofluorescence data
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
GO_REF:0000120
Combined Automated Annotation using Multiple IEA Methods
PMID:20603078
The cytoplasmic adaptor protein Dok7 activates the receptor tyrosine kinase MuSK via dimerization.
PMID:32296183
A reference map of the human binary protein interactome.
PMID:14702039
Complete sequencing and characterization of 21,243 full-length human cDNAs.
PMID:15489334
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PMID:15815621
Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
PMID:16794080
The muscle protein Dok-7 is essential for neuromuscular synaptogenesis.
PMID:16917026
Dok-7 mutations underlie a neuromuscular junction synaptopathy.
PMID:17439981
Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes.
PMID:19261599
Germline mutation in DOK7 associated with fetal akinesia deformation sequence.
PMID:20012313
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7.
PMID:21041412
Dok-7 regulates neuromuscular synapse formation by recruiting Crk and Crk-L.
PMID:22661499
The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome.
UniProt:Q18PE1
UniProtKB Q18PE1 (DOK7_HUMAN)
https://www.proteinatlas.org/ENSG00000175920-DOK7/subcellular
Subcellular - DOK7 - The Human Protein Atlas