Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
220164
Gene name Gene Name - the full gene name approved by the HGNC.
Docking protein 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DOK6
Synonyms (NCBI Gene) Gene synonyms aliases
DOK5L, HsT3226
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18q22.2
Summary Summary of gene provided in NCBI Entrez Gene.
DOK6 is a member of the DOK (see DOK1; MIM 602919) family of intracellular adaptors that play a role in the RET (MIM 164761) signaling cascade (Crowder et al., 2004 [PubMed 15286081]).[supplied by OMIM, Mar 2008]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018286 hsa-miR-335-5p Microarray 18185580
MIRT023914 hsa-miR-1-3p Microarray 18668037
MIRT721835 hsa-miR-410-3p HITS-CLIP 19536157
MIRT721834 hsa-miR-5011-5p HITS-CLIP 19536157
MIRT721833 hsa-miR-141-5p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16273093, 20565848, 25416956, 32296183
GO:0005737 Component Cytoplasm IBA
GO:0005829 Component Cytosol TAS
GO:0007169 Process Cell surface receptor protein tyrosine kinase signaling pathway IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611402 28301 ENSG00000206052
Protein
UniProt ID Q6PKX4
Protein name Docking protein 6 (Downstream of tyrosine kinase 6)
Protein function DOK proteins are enzymatically inert adaptor or scaffolding proteins. They provide a docking platform for the assembly of multimolecular signaling complexes. DOK6 promotes Ret-mediated neurite growth. May have a role in brain development and/or
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02174 IRS 135 232 PTB domain (IRS-1 type) Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in fetal and adult brain. Highly expressed in the cerebellum. Weak expression in kidney, spinal cord and testis. {ECO:0000269|PubMed:15286081}.
Sequence
MASNFNDIVKQGYVKIRSRKLGIFRRCWLVFKKASSKGPRRLEKFPDEKAAYFRNFHKVT
ELHNIKNITRLPRETKKHAVAIIFHDETSKTFACESELEAEEWCKHLCMECLGTRLNDIS
LGEPDLLAAGVQREQNERFNVYLMPTPNLDIYGECTMQITHENIYLWDIHNAKVKLVMWP
LSSLRRYGRDSTWFTFESGRMCDTGEGLFTFQTREGEMIYQKVHSATLAIAE
QHERLMLE
MEQKARLQTSLTEPMTLSKSISLPRSAYWHHITRQNSVGEIYSLQGHGFGSSKMSRAQTF
PSYAPEQSEEAQQPLSRSSSYGFSYSSSLIQ
Sequence length 331
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    RET signaling
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Breast Cancer Breast cancer N/A N/A GWAS
Dementia Dementia N/A N/A GWAS
Glioblastoma Glioblastoma N/A N/A GWAS
Ischemic Stroke Ischemic stroke N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 31486300
Hirschsprung Disease Associate 34545688
Leukemia Myeloid Acute Associate 31486300
Leukemia Promyelocytic Acute Associate 31486300
Stomach Neoplasms Associate 31486300