PRKX - protein kinase cAMP-dependent X-linked catalytic subunit Gene

Also Known as PKX1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5613

About PRKX

Cytogenetic location: Xp22.33 Genomic coordinates (GRCh38): X:3,604,340-3,713,649 (from NCBI)

This gene has 4 transcripts (splice variants), 193 orthologues and 5 paralogues. Broad expression in thyroid (RPKM 22.9), kidney (RPKM 7.3) and 20 other tissues.

Summary

This gene encodes a serine threonine protein kinase that has similarity to the catalytic subunit of cyclic AMP dependent protein kinases. The encoded protein is developmentally regulated and may be involved in renal epithelial morphogenesis. This protein may also be involved in macrophage and granulocyte maturation. Abnormal recombination between this gene and a related pseudogene on chromosome Y is a frequent cause of sex reversal disorder in XX males and XY females. Pseudogenes of this gene are found on chromosomes X, 15 and Y. [provided by RefSeq, Feb 2010]

PRKX Products (1)

mRNA Protein Name
NM_005044.5 NP_005035.1 cAMP-dependent protein kinase catalytic subunit PRKX
Molecular Function GO Annotation Evidence Références Source
enables cAMP-dependent protein kinase activity IDA
IDA: Inferred from direct assay
10026146 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16491121 GOA
Biological Process GO Annotation Evidence Références Source
involved in angiogenesis IMP
IMP: Inferred from mutant phenotype
21684272 GOA
involved in cell adhesion IMP
IMP: Inferred from mutant phenotype
21684272 GOA
involved in cell-substrate adhesion IMP
IMP: Inferred from mutant phenotype
16491121 GOA
involved in endothelial cell migration IMP
IMP: Inferred from mutant phenotype
21684272 GOA
involved in endothelial cell proliferation IMP
IMP: Inferred from mutant phenotype
21684272 GOA
involved in epithelial tube morphogenesis IDA
IDA: Inferred from direct assay
17980165 GOA
involved in kidney morphogenesis IDA
IDA: Inferred from direct assay
17980165 GOA
involved in myeloid cell differentiation IDA
IDA: Inferred from direct assay
9860982 GOA
involved in peptidyl-serine phosphorylation IDA
IDA: Inferred from direct assay
16491121 GOA
involved in protein autophosphorylation IDA
IDA: Inferred from direct assay
10026146 GOA
involved in regulation of cell adhesion IDA
IDA: Inferred from direct assay
17980165 GOA
involved in regulation of cell migration IDA
IDA: Inferred from direct assay
17980165 GOA
involved in regulation of epithelial cell differentiation involved in kidney development IDA
IDA: Inferred from direct assay
17980165 GOA
Cellular Component GO Annotation Evidence Références Source
located in cytoplasm IDA
IDA: Inferred from direct assay
10026146 GOA
located in nucleus IDA
IDA: Inferred from direct assay
10026146 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

PRKX Protein Structure

Pkinase

Pkinase: Protein kinase domain (51 - 303)

  • 0
  • 100
  • 200
  • 300
  • 358 a.a.
Protein Preferred Names Protein Names

cAMP-dependent protein kinase catalytic subunit PRKX

  • protein kinase PKX1

PRKX Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
PRKX P51817 HSP90AB1 Homo sapiens P08238 32707033
Intra
PRKX P51817 HSP90AB1 Homo sapiens P08238 22939624
Intra
PRKX P51817 PRKAR1A Homo sapiens P10644
Y2H
16491121
Intra
PRKX P51817 PRKAR1A Homo sapiens P10644 16491121
Intra
PRKX P51817 GPKOW Homo sapiens Q92917 16491121
Intra
PRKX P51817 SMAD6 Homo sapiens O43541 16491121
Intra
PRKX P51817 SMAD6 Homo sapiens O43541 16491121
Intra
PRKX P51817 SMAD6 Homo sapiens O43541
Y2H
16491121
Intra
PRKX P51817 SMAD6 Homo sapiens O43541 16491121
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Asbestos-Related Lung Carcinoma
Breast Ductal Adenoma
Primary Pigmented Nodular Adrenocortical Disease
  • Ppnad

  • Primary Pigmented Nodular Adrenal Dysplasia

  • Pigmented Nodular Adrenocortical Disease, Primary, 2

  • Pigmented Nodular Adrenocortical Disease, Primary, 1

Acth-Independent Macronodular Adrenal Hyperplasia
  • Acth-Independent Macronodular Adrenocortical Hyperplasia

  • Adrenocorticotropic Hormone-Independent Macronodular Adrenal Hyperplasia

  • Corticotropin-Independent Macronodular Adrenal Hyperplasia

  • Cushing Syndrome Due To Macronodular Adrenal Hyperplasia

  • AIMAH1

  • Aimah

  • Massive Macronodular Adrenocortical Disease

  • Mmad

  • Primary Macronodular Adrenal Hyperplasia

  • Cushing Syndrome, Adrenal, Due To Aimah

  • Primary Bilateral Macronodular Adrenal Hyperplasia

  • Acth-Independent Macronodular Adrenal Hyperplasia 1

  • Acth-Independent Cushing Syndrome

  • Adrenal Cushing Syndrome Due To Aimah

  • Acth-Independent Macronodular Adrenal Hyperplasia 2

Polycystic Kidney Disease
  • Polycystic Kidney Diseases

  • Pkd

  • Polycystic Renal Disease

  • Kidney Disease, Polycystic

  • Polycystic Kidney, Autosomal Dominant

Carney Complex Variant
  • Carney Complex

  • Carney Syndrome

  • Carney Complex, Type 1

  • Lamb Syndrome

  • Name Syndrome

  • Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome

  • Carney Complex - Trismus - Pseudocamptodactyly Syndrome

  • Carney Complex, Type 2

  • Car

  • Cnc1

  • Carney Myxoma-Endocrine Complex

  • Myxoma - Spotty Pigmentation - Endocrine Overactivity

  • Myxoma, Spotty Pigmentation, And Endocrine Overactivity

  • Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome

  • Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome

  • Carney Complex-Trismus-Pseudocamptodactyly Syndrome

  • CACOV

Fibrolamellar Carcinoma
  • Fibrolamellar Hepatocellular Carcinoma

  • Fhcc

  • Fibrolamellar Hepatocarcinoma

  • Hepatocellular Carcinoma, Fibrolamellar

  • Oncocytic Hepatocellular Tumor

  • Eosinophilic Glassy Cell Hepatoma

  • Eosinophilic Hepatocellular Carcinoma With Lamellar Fibrosis

  • Fl-Hcc

  • Fibrolamellar Oncocytic Hepatoma

  • Hepatocellular Carcinoma With Increased Stromal Fibrosis

  • Polygonal Cell Hepatocellular Carcinoma With Fibrous Stroma

Breast Adenoma
  • Ademoma - Breast

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
Mus musculus PRKX MGD MGI:1309999
Rattus norvegicus PRKX RGD RGD:1564076
Canis familiaris PRKX VGNC VGNC:54833
Others PRKX NCBI