Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23012
Gene name Gene Name - the full gene name approved by the HGNC.
Serine/threonine kinase 38 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
STK38L
Synonyms (NCBI Gene) Gene synonyms aliases
NDR2
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12p11.23
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019964 hsa-miR-375 Microarray 20215506
MIRT022750 hsa-miR-124-3p Microarray 18668037
MIRT045849 hsa-miR-130a-3p CLASH 23622248
MIRT063948 hsa-miR-205-5p HITS-CLIP 22473208
MIRT063948 hsa-miR-205-5p HITS-CLIP 22473208
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:0000287 Function Magnesium ion binding IDA 15067004
GO:0000287 Function Magnesium ion binding IEA
GO:0003779 Function Actin binding IEA
GO:0004672 Function Protein kinase activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615836 17848 ENSG00000211455
Protein
UniProt ID Q9Y2H1
Protein name Serine/threonine-protein kinase 38-like (EC 2.7.11.1) (NDR2 protein kinase) (Nuclear Dbf2-related kinase 2)
Protein function Involved in the regulation of structural processes in differentiating and mature neuronal cells.
PDB 5XQZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 90 383 Protein kinase domain Domain
PF00433 Pkinase_C 402 443 Protein kinase C terminal domain Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed with highest levels observed in the thymus. {ECO:0000269|PubMed:15067004}.
Sequence
Sequence length 464
Interactions View interactions
<
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
Dementia Dementia N/A N/A GWAS
Glioma Glioma N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Developmental Disabilities Associate 37563198
Kallmann Syndrome Associate 37563198
Microsatellite Instability Associate 30108113
Ovarian Neoplasms Associate 30392041