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Gene Gene information from NCBI Gene database.
Entrez ID 51657
Gene name Serine/threonine/tyrosine interacting like 1
Gene symbol STYXL1
Synonyms (NCBI Gene)
DUSP24MK-STYXMKSTYX
Chromosome 7
Chromosome location 7q11.23
miRNA miRNA information provided by mirtarbase database.
18 Show/Hide all (18)
miRTarBase ID miRNA Experiments Reference
MIRT1402109 hsa-miR-125a-3p CLIP-seq
MIRT1402110 hsa-miR-1291 CLIP-seq
MIRT1402111 hsa-miR-3176 CLIP-seq
MIRT1402112 hsa-miR-328 CLIP-seq
MIRT1402113 hsa-miR-329 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17 Show/Hide all (17)
GO ID Ontology Definition Evidence Reference
GO:0001691 Function Pseudophosphatase activity IBA
GO:0001691 Function Pseudophosphatase activity IMP 20180778, 23163895
GO:0005515 Function Protein binding IPI 19026618, 20180778
GO:0005739 Component Mitochondrion IBA
GO:0005739 Component Mitochondrion IDA 21262771
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616695 18165 ENSG00000127952
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y6J8
Protein name Serine/threonine/tyrosine-interacting-like protein 1 (Dual specificity phosphatase inhibitor MK-STYX) (Dual specificity protein phosphatase 24) (Inactive dual specificity protein phosphatase MK-STYX) (Map kinase phosphatase-like protein MK-STYX)
Protein function Catalytically inactive phosphatase (PubMed:20180778, PubMed:23163895). By binding to G3BP1, inhibits the formation of G3BP1-induced stress granules (PubMed:20180778, PubMed:23163895). Does not act by protecting the dephosphorylation of G3BP1 at
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00581 Rhodanese 9 → 137 Rhodanese-like domain Domain
PF00782 DSPc 168 → 299 Dual specificity phosphatase, catalytic domain Domain
Sequence
Sequence length 313
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 Reference Evidence Score
STYXL1-related disorder Likely benign; Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (9)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 32271415 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes mellitus Pubtator 36360783 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Diabetes mellitus, type 2 Pubtator 37679740 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma BEFREE 31146910
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 31146910
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioma Glioma BEFREE 31146910
★★★★★
★☆☆☆☆
Found in Text Mining only
Infertility Male Male infertility Pubtator 38168070 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Moderate intellectual disability Mental retardation BEFREE 25724587, 30472486
★★★★★
★☆☆☆☆
Found in Text Mining only
Precursor B-cell lymphoblastic leukemia Lymphoblastic Leukemia BEFREE 25326153
★★★★★
★☆☆☆☆
Found in Text Mining only