Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
149420
Gene name Gene Name - the full gene name approved by the HGNC.
PDLIM1 interacting kinase 1 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PDIK1L
Synonyms (NCBI Gene) Gene synonyms aliases
CLIK1L, STK35L2
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.11
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT003816 hsa-miR-373-3p Microarray 15685193
MIRT016218 hsa-miR-590-3p Sequencing 20371350
MIRT024137 hsa-miR-221-3p Sequencing 20371350
MIRT050716 hsa-miR-18a-5p CLASH 23622248
MIRT049117 hsa-miR-92a-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0004672 Function Protein kinase activity IBA
GO:0004672 Function Protein kinase activity IEA
GO:0004674 Function Protein serine/threonine kinase activity IEA
GO:0005515 Function Protein binding IPI 22939624, 25036637, 25416956, 28514442, 32296183, 32707033, 33961781
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610785 18981 ENSG00000175087
Protein
UniProt ID Q8N165
Protein name Serine/threonine-protein kinase PDIK1L (EC 2.7.11.1) (PDLIM1-interacting kinase 1-like)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 8 327 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in liver, kidney, pancreas, spleen, thymus and prostate. {ECO:0000269|PubMed:14631099}.
Sequence
Sequence length 341
Interactions View interactions
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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
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Anophthalmia with pulmonary hypoplasia Associate 32029502
Breast Neoplasms Associate 35069784
Leukemia Myeloid Acute Associate 35021089
Prostatic Neoplasms Associate 33404048