Gene

SGK1

Species
Homo sapiens
Symbol
SGK1
Name
serum/glucocorticoid regulated kinase 1
Synonyms
  • serine/threonine protein kinase SGK
  • serine/threonine-protein kinase Sgk1
Biotype
protein coding gene
Automated Description
Enables protein serine/threonine/tyrosine kinase activity. Predicted to be involved in intracellular signal transduction and neuron projection morphogenesis. Predicted to act upstream of or within several processes, including cellular response to aldosterone; cellular response to insulin stimulus; and positive regulation of sodium ion transport. Located in cytosol and nuclear speck. Implicated in hypertension. Biomarker of granulosa cell tumor; mucinous cystadenocarcinoma; and serous cystadenocarcinoma.
RGD Description
This gene encodes a serine/threonine protein kinase that plays an important role in cellular stress response. This kinase activates certain potassium, sodium, and chloride channels, suggesting an involvement in the regulation of processes such as cell survival, neuronal excitability, and renal sodium excretion. High levels of expression of this gene may contribute to conditions such as hypertension and diabetic nephropathy. Several alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR24351
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Mus musculusSgk110 of 10YesYes  
Rattus norvegicusSgk110 of 10YesYes  
Xenopus laevissgk1.S1 of 1YesYes           
Xenopus laevissgk1.L1 of 1YesYes           
Xenopus tropicalissgk18 of 9YesYes   
Danio reriosgk19 of 10YesYes  
Caenorhabditis eleganssgk-18 of 9YesNo   
Saccharomyces cerevisiae S288CYPK14 of 9YesYes   
Saccharomyces cerevisiae S288CYPK23 of 9NoYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
SGK3143478667 of 8  
C8orf44-SGK3143478667 of 8  
SGK2236886718 of 8  
AKT1352454383 of 8  
PRKCE461048322 of 8  
PRKCA557849332 of 8  
PRKCH657150332 of 8  
AKT3743459453 of 8  
PRKCI855151342 of 8  
PRKCD958748322 of 8  
AKT21045056423 of 8  
PRKCG1154350342 of 8  
PRKCB1252951342 of 8  
PKN11350352342 of 8  
LATS21455945283 of 8  
LATS11561243262 of 8  
PRKCQ1647151382 of 8  
PKN31747851362 of 8  
PRKCZ1844751342 of 8  
PKN21943152362 of 8  
STK382047748282 of 8  
DMPK2141548343 of 8  
STK38L2251942252 of 8  
MAST32340850323 of 8  
MAST42441550303 of 8  
MAST22539151313 of 8  
MAST12635652342 of 8  
PDPK12731657392 of 8  
STK32B2833651343 of 8  
STK32A2933751313 of 8  
STK32C3030852343 of 8  
MASTL3127649332 of 8  

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
Phenotype Term
Annotation details
References
Abnormal systemic blood pressure
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Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume
Species
Gene
Association
Disease Qualifier
Disease
Evidence
Source
Based On
References
No records match query. Try removing filters.
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    Alleles and Variants

    Genome location
    Assembly version
    GRCh38
    Viewer Help
    Data currently unavailable; sequence viewer under construction
    Allele/Variant Symbol
    Allele Synonyms
    Category
    Variant
    Variant type
    Molecular consequence
    Has Disease Annotations
    Has Phenotype Annotations
    NC_000006.12:g.134175584C>Tvariant
    SNP
    • intron variant
    NC_000006.12:g.134170390C>Gvariant
    SNP
    • missense variant
    NC_000006.12:g.134261969G>Cvariant
    SNP
    • missense variant
    NC_000006.12:g.134170402C>Tvariant
    SNP
    • missense variant
    NC_000006.12:g.134174596A>Gvariant
    SNP
    • intron variant
    NC_000006.12:g.134207381T>Cvariant
    SNP
    • synonymous variant
    NC_000006.12:g.134173085G>Avariant
    SNP
    • missense variant
    NC_000006.12:g.134173523G>Avariant
    SNP
    • missense variant
    NC_000006.12:g.134170333C>Tvariant
    SNP
    • missense variant
    NC_000006.12:g.134170319G>Avariant
    SNP
    • synonymous variant
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    Transgenic Alleles

    No data available

    Models

    No data available

    Sequence Feature Viewer

    Genome location
    Assembly version
    GRCh38
    Viewer Help
    Data currently unavailable; sequence viewer under construction

    Sequence Details

    Transcript: Mode:

    Expression

    Primary Sources
    None
    Other Sources
    Must provide at least one subject
    Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

    Molecular Interactions

    SGK1 molecule type
    Interactor gene
    Interactor species
    Interactor molecule type
    Detection method
    Source
    Reference
    protein
    AKT1S1Homo sapiens
    protein
    affinity chromatography technology
    PMID:18570873
    protein
    ARL5BHomo sapiens
    protein
    affinity chromatography technology
    PMID:28514442
    protein
    ARL5BHomo sapiens
    protein
    affinity chromatography technology
    PMID:26186194
    protein
    ASPGHomo sapiens
    protein
    affinity chromatography technology
    PMID:21063096
    protein
    ASPGHomo sapiens
    protein
    two hybrid
    PMID:21063096
    protein
    ASPGHomo sapiens
    protein
    affinity chromatography technology
    PMID:21063096
    protein
    ASPGHomo sapiens
    protein
    pull down
    PMID:21063096
    protein
    CAMKK2Homo sapiens
    protein
    affinity chromatography technology
    PMID:12628440
    protein
    CARHSP1Homo sapiens
    protein
    pull down
    PMID:15910284
    protein
    CD40Homo sapiens
    protein
    affinity chromatography technology
    PMID:17353931
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    Genetic Interactions

    SGK1 role
    SGK1 genetic perturbation
    Interactor gene
    Interactor species
    Interactor role
    Interactor genetic perturbation
    Interaction type
    Phenotype or trait
    Source
    Reference
    unspecified role
    AKT3Homo sapiens
    unspecified role
    negative genetic interaction (sensu BioGRID)
    PMID:34857952
    unspecified role
    RPS6KB1Homo sapiens
    unspecified role
    negative genetic interaction (sensu BioGRID)
    PMID:34857952
    suppressor gene
    YPK1Saccharomyces cerevisiae
    suppressed gene
    dosage rescue (sensu BioGRID)
    • viability, complete rescue
    PMID:20516150
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