STOX1 - storkhead box 1 Gene

Also Known as C10orf24

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 219736

About STOX1

Cytogenetic location: 10q22.1 Genomic coordinates (GRCh38): 10:68,827,531-68,895,432 (from NCBI)

This gene has 5 transcripts (splice variants), 200 orthologues, 1 paralogue and is associated with 2 phenotypes. Broad expression in brain (RPKM 2.8), fat (RPKM 2.4) and 21 other tissues.

Summary

The protein encoded by this gene may function as a DNA binding protein. Mutations in this gene are associated with pre-eclampsia/eclampsia 4 (PEE4). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

STOX1 Products (4)

mRNA Protein Name
NM_001130159.3 NP_001123631.1 storkhead-box protein 1 isoform b
NM_001130160.3 NP_001123632.1 storkhead-box protein 1 isoform c
NM_001130161.4 NP_001123633.1 storkhead-box protein 1 isoform a
NM_152709.5 NP_689922.3 storkhead-box protein 1 isoform a
Molecular Function GO Annotation Evidence Verweise Source
enables RNA polymerase II transcription regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
22253775 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in cellular response to nitrosative stress IMP
IMP: Inferred from mutant phenotype
24738702 GOA
involved in negative regulation of gene expression IMP
IMP: Inferred from mutant phenotype
22253775 GOA
involved in positive regulation of G1/S transition of mitotic cell cycle IMP
IMP: Inferred from mutant phenotype
22253775 GOA
involved in positive regulation of G2/M transition of mitotic cell cycle IMP
IMP: Inferred from mutant phenotype
22253775 GOA
involved in positive regulation of cyclin-dependent protein kinase activity IMP
IMP: Inferred from mutant phenotype
22253775 GOA
involved in positive regulation of gene expression IMP
IMP: Inferred from mutant phenotype
22253775 GOA
involved in positive regulation of peptidyl-serine phosphorylation IMP
IMP: Inferred from mutant phenotype
22995177 GOA
involved in positive regulation of peptidyl-threonine phosphorylation IMP
IMP: Inferred from mutant phenotype
22995177 GOA
involved in regulation of gene expression IMP
IMP: Inferred from mutant phenotype
24738702 GOA
involved in regulation of mitochondrial DNA metabolic process IMP
IMP: Inferred from mutant phenotype
24738702 GOA
involved in regulation of mitochondrial membrane potential IMP
IMP: Inferred from mutant phenotype
24738702 GOA
involved in regulation of mitochondrion organization IMP
IMP: Inferred from mutant phenotype
24738702 GOA
involved in regulation of response to oxidative stress IMP
IMP: Inferred from mutant phenotype
24738702 GOA
involved in regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
24738702 GOA
Cellular Component GO Annotation Evidence Verweise Source
located in centrosome IDA
IDA: Inferred from direct assay
22253775 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
22253775 GOA
located in nucleus IDA
IDA: Inferred from direct assay
22253775 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

STOX1 Protein Structure

Stork_head

Stork_head: Winged helix Storkhead-box1 domain (111 - 190)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 989 a.a.
Protein Preferred Names Protein Names

storkhead-box protein 1

  • winged-helix domain-containing protein

STOX1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
STOX1 Q6ZVD7 BANP Homo sapiens Q8N9N5-2 32296183
Intra
STOX1 Q6ZVD7 ADARB1 Homo sapiens P78563-4 32296183
Intra
STOX1 Q6ZVD7 ADARB1 Homo sapiens P78563-4 32296183
Intra
STOX1 Q6ZVD7 GORASP2 Homo sapiens Q9H8Y8 31515488
Intra
STOX1 Q6ZVD7 GORASP2 Homo sapiens Q9H8Y8 25416956
Intra
STOX1 Q6ZVD7 GORASP2 Homo sapiens Q9H8Y8 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Preeclampsia/Eclampsia 4
  • PEE4

  • Pre-Eclampsia/Eclampsia 4

  • Gestational Proteinuric Hypertension

  • Preeclampsia/Eclampsia, Type 4

  • Preeclampsia Eclampsia 4

Eclampsia
  • Eclampsia In Puerperium

  • Postpartum Eclampsia

  • Eclampsia, Postpartum

  • Puerperal Eclampsia

Pre-Eclampsia
  • Preeclampsia

  • Gestational Hypertension

  • Hypertension Induced By Pregnancy

  • Pre-Eclamptic Toxaemia

  • Pregnancy Associated Hypertension

  • Proteinuric Hypertension Of Pregnancy

  • Hypertension, Pregnancy-Induced, Susceptibility To

  • Preeclampsia/Eclampsia

  • Pregnancy Toxemia

  • Toxaemia Of Pregnancy

  • Gestational Proteinuric Hypertension

  • Pregnancy-Induced Hypertension

  • Toxemia Of Pregnancy

  • Preeclampsia, Susceptibility To

  • Transient Hypertension Of Pregnancy

  • Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria

  • Gestational Hypertension Nos

  • Mild Proteinuric Hypertension Of Pregnancy

  • Pih - [Pregnancy-Induced Hypertension]

  • Pregnancy-Induced Hypertension Nos

  • Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria

  • Pe - [Pre-Eclampsia]

  • Pre-Eclampsia Nos

  • Pre-Eclamptic Nos

  • Pregnancy Pre-Eclampsia

  • Puerperal Pre-Eclampsia

  • Pre-Eclampsia Toxaemia

  • Toxaemia In Pregnancy

  • Pet - [Pre-Eclamptic Toxaemia]

  • Maternal Toxaemia

Severe Pre-Eclampsia
  • Severe Preeclampsia

  • Antepartum Severe Pre-Eclampsia

  • Postpartum Severe Pre-Eclampsia

  • Severe Pre-Eclampsia, With Delivery

  • Severe Toxemia

  • Severe Pre-Eclampsia, Antepartum Condition Or Complication

  • Severe Pre-Eclampsia, Postpartum Condition Or Complication

  • Severe Puerperal Pre-Eclampsia

  • Severe Pre-Eclamptic Toxaemia

  • Severe Pet - [Pre-Eclamptic Toxaemia]

Patau Syndrome
  • Trisomy 13

  • Complete Trisomy 13 Syndrome

  • Trisomy 13 Syndrome

  • D1 Trisomy

  • Patau'S Syndrome

  • Complete Trisomy 13

  • Chromosome 13, Trisomy 13 Complete

  • D Trisomy Syndrome

  • Bartholin-Patau Syndrome

  • Chromosome 13 Duplication

  • D1 Trisomy Syndrome

  • D>1< Trisomy Syndrome

  • Patau

  • Chromosome 13 Trisomy

  • Abnormal Autosomes 13

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus STOX1 VGNC VGNC:35414
Canis familiaris STOX1 VGNC VGNC:49791
Macaca mulatta STOX1 VGNC VGNC:78197
Mus musculus STOX1 MGD MGI:2684909
Rattus norvegicus STOX1 RGD RGD:1310622
Others STOX1 NCBI