Gene Gene information from NCBI Gene database.
Entrez ID 285193
Gene name Dual specificity phosphatase 28
Gene symbol DUSP28
Synonyms (NCBI Gene)
DUSP26VHP
Chromosome 2
Chromosome location 2q37.3
miRNA miRNA information provided by mirtarbase database.
166
miRTarBase ID miRNA Experiments Reference
MIRT643992 hsa-miR-4328 HITS-CLIP 23824327
MIRT643991 hsa-miR-6752-3p HITS-CLIP 23824327
MIRT643990 hsa-miR-212-5p HITS-CLIP 23824327
MIRT643989 hsa-miR-3189-3p HITS-CLIP 23824327
MIRT643988 hsa-miR-4469 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0004721 Function Phosphoprotein phosphatase activity IEA
GO:0004722 Function Protein serine/threonine phosphatase activity IEA
GO:0004725 Function Protein tyrosine phosphatase activity IEA
GO:0016311 Process Dephosphorylation IDA 24531476
GO:0016787 Function Hydrolase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q4G0W2
Protein name Dual specificity phosphatase 28 (EC 3.1.3.16) (EC 3.1.3.48)
Protein function Has phosphatase activity with the synthetic substrate 6,8-difluoro-4-methylumbelliferyl phosphate (in vitro) (PubMed:24531476, PubMed:29121083). Has almost no detectable activity with phosphotyrosine, even less activity with phosphothreonine and
PDB 5Y15 , 5Y16
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00782 DSPc 26 156 Dual specificity phosphatase, catalytic domain Domain
Sequence
Sequence length 176
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
MULTIPLE SCLEROSIS CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Alzheimer Disease Alzheimer disease Pubtator 26924229, 32614981 Associate
★☆☆☆☆
Found in Text Mining only
Anaplastic thyroid carcinoma Anaplastic thyroid cancer BEFREE 16924234
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety Disorder BEFREE 31541642
★☆☆☆☆
Found in Text Mining only
Anxiety Disorders Anxiety Disorder BEFREE 31541642
★☆☆☆☆
Found in Text Mining only
Astrocytoma Astrocytoma Pubtator 27586084 Associate
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Non-Insulin-Dependent Diabetes Mellitus BEFREE 31700183
★☆☆☆☆
Found in Text Mining only
Diabetic Nephropathy Diabetic Nephropathy BEFREE 31155289
★☆☆☆☆
Found in Text Mining only
Epilepsy, Temporal Lobe Epilepsy BEFREE 30098387
★☆☆☆☆
Found in Text Mining only
Fatty Liver Fatty Liver BEFREE 30582764
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma BEFREE 19043453
★☆☆☆☆
Found in Text Mining only