Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55816
Gene name Gene Name - the full gene name approved by the HGNC.
Docking protein 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DOK5
Synonyms (NCBI Gene) Gene synonyms aliases
C20orf180, IRS-6, IRS6
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q13.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the DOK family of membrane proteins, which are adapter proteins involved in signal transduction. The encoded protein interacts with phosphorylated receptor tyrosine kinases to mediate neurite outgrowth and a
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT943132 hsa-miR-10a CLIP-seq
MIRT943133 hsa-miR-10b CLIP-seq
MIRT943134 hsa-miR-198 CLIP-seq
MIRT943135 hsa-miR-30a CLIP-seq
MIRT943136 hsa-miR-30b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005829 Component Cytosol TAS
GO:0007169 Process Transmembrane receptor protein tyrosine kinase signaling pathway IEA
GO:0007411 Process Axon guidance TAS
GO:0043410 Process Positive regulation of MAPK cascade IEA
GO:0051386 Process Regulation of neurotrophin TRK receptor signaling pathway IMP 23954828
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608334 16173 ENSG00000101134
Protein
UniProt ID Q9P104
Protein name Docking protein 5 (Downstream of tyrosine kinase 5) (Insulin receptor substrate 6) (IRS-6) (IRS6)
Protein function DOK proteins are enzymatically inert adaptor or scaffolding proteins. They provide a docking platform for the assembly of multimolecular signaling complexes. DOK5 functions in RET-mediated neurite outgrowth and plays a positive role in activatio
PDB 1J0W
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: Highest expression in skeletal muscle, lower in brain, heart and kidney. Also detected in activated peripheral blood T-lymphocytes. {ECO:0000269|PubMed:12595900, ECO:0000269|PubMed:12730241}.
Sequence
MASNFNDIVKQGYVRIRSRRLGIYQRCWLVFKKASSKGPKRLEKFSDERAAYFRCYHKVT
ELNNVKNVARLPKSTKKHAIGIYFNDDTSKTFACESDLEADEWCKVLQMECVGTRINDIS
LGEPDLLATGVEREQSERFNVYLMPSPNLDVHGECALQITYEYICLWDVQNPRVKLISWP
LSALRRYGRDTTWFTFEAGRMCETGEGLFIFQTRDGEAIYQKVHSAALAIAE
QHERLLQS
VKNSMLQMKMSERAASLSTMVPLPRSAYWQHITRQHSTGQLYRLQDVSSPLKLHRTETFP
AYRSEH
Sequence length 306
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    RET signaling
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Celiac disease Celiac disease GWAS
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Bipolar Disorder Associate 20215924
Carcinoma Hepatocellular Associate 32148377
Colorectal Neoplasms Associate 28540987
Diabetes Mellitus Type 2 Associate 20187968, 22152676
Myopathies Structural Congenital Associate 35036444
Neoplasms Associate 28540987, 35036444
Obesity Associate 20187968
Pheochromocytoma Associate 20534969
Stomach Neoplasms Associate 35036444