HYOU1 - hypoxia up-regulated 1 Gene

Also Known as IMD59; Grp170; HSP12A; ORP150; GRP-170; ORP-150

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10525

About HYOU1

Cytogenetic location: 11q23.3 Genomic coordinates (GRCh38): 11:119,044,188-119,057,205 (from NCBI)

This gene has 29 transcripts (splice variants), 1 gene allele, 209 orthologues, 13 paralogues and is associated with 1 phenotype. Broad expression in thyroid (RPKM 93.3), testis (RPKM 55.6) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the heat shock protein 70 family. This gene uses alternative transcription start sites. A cis-acting segment found in the 5' UTR is involved in stress-dependent induction, resulting in the accumulation of this protein in the endoplasmic reticulum (ER) under hypoxic conditions. The protein encoded by this gene is thought to play an important role in protein folding and secretion in the ER. Since suppression of the protein is associated with accelerated Apoptosis, it is also suggested to have an important cytoprotective role in hypoxia-induced cellular perturbation. This protein has been shown to be up-regulated in tumors, especially in breast tumors, and thus it is associated with tumor invasiveness. This gene also has an alternative translation initiation site, resulting in a protein that lacks the N-terminal signal peptide. This signal peptide-lacking protein, which is only 3 Amino acids shorter than the mature protein in the ER, is thought to have a housekeeping function in the cytosol. In rat, this protein localizes to both the ER by a carboxy-terminal peptide sequence and to mitochondria by an amino-terminal targeting signal. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]

HYOU1 Products (3)

mRNA Protein Name
NM_001130991.3 NP_001124463.1 hypoxia up-regulated protein 1 isoform 1 precursor
NM_001411041.1 NP_001397970.1 hypoxia up-regulated protein 1 isoform 2 precursor
NM_006389.5 NP_006380.1 hypoxia up-regulated protein 1 isoform 1 precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
26496610 GOA
Biological Process GO Annotation Evidence References Source
involved in cellular response to hypoxia IDA
IDA: Inferred from direct assay
10837345 GOA
involved in cellular response to hypoxia IEP
IEP: Inferred from expression pattern
9020069 GOA
involved in endoplasmic reticulum to Golgi vesicle-mediated transport IDA
IDA: Inferred from direct assay
10837345 GOA
involved in negative regulation of hypoxia-induced intrinsic apoptotic signaling pathway IDA
IDA: Inferred from direct assay
10037731 GOA
involved in response to endoplasmic reticulum stress IEP
IEP: Inferred from expression pattern
9020069 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

HYOU1 Protein Structure

HSP70

HSP70: Hsp70 protein (36 - 809)

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

hypoxia up-regulated protein 1

  • 150 kDa oxygen-regulated protein

HYOU1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
HYOU1 Q9Y4L1 HSPA5 Homo sapiens P11021 33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant HYOU1 Proteins

Cat. No. Product Name Accession Purity
HY-P70943 HYOU1 Protein, Human (HEK293, His) Q9Y4L1-1 (M695-L999) ≥ 95%, as determined by reducing SDS-PAGE.

HYOU1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81733 ORP150 Antibody (YA1478) WB, IHC-P Human, Mouse, Rat
HY-P81733A ORP150 Antibody (YA1478)(PBS only) WB, IHC-P Human, Mouse, Rat

Related Diseases

Diseases Alias
Immunodeficiency 59 And Hypoglycemia
  • Granulocytopenia With Immunoglobulin Abnormality

  • IMD59

  • Immunodeficiency 59

  • Granulocytopenia With Immunoglobin Abnormality

B Cell And Dendritic Cell Deficiency
Dendritic Cell Deficiency
Granulocytopenia
  • Agranulocytosis

Hypoglycemia
  • Hypoglycaemia

  • Low Blood Sugar

  • Hypoglycaemia Nos

  • Spontaneous Hypoglycaemia

  • Nondiabetic Hypoglycaemia

  • Hypoglycaemic Disorder Nos

  • Hypoglycaemic Syndrome

Combined Immunodeficiency
  • Combined T Cell And B Cell Immunodeficiency

  • Congenital Combined Immunodeficiency

  • Syndrome With Combined Immunodeficiency

  • Combined T And B Cell Immunodeficiency

  • Combined Immunity Deficiency

  • Combined Immunodeficiency Syndrome

  • Combined T-Cell And B-Cell Immunodeficiency

  • Lymphopenic Agammaglobulinaemia

Marinesco-Sjogren Syndrome
  • Marinesco-Sjögren Syndrome

  • MSS

  • Marinesco-Garland Syndrome

  • Garland-Moorhouse Syndrome

  • Hereditary Oligophrenic Cerebello-Lental Degeneration

  • Oligophrenic Cerebellolenticular Degeneration

  • Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism

  • Marinesco-Sjogren Syndrome-Myopathy

  • Marinesco-Sjogren-Garland Syndrome

  • Marinesco-Sjoegren Syndrome

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
Canis familiaris HYOU1 VGNC VGNC:53417
Rattus norvegicus HYOU1 RGD RGD:621146
Mus musculus HYOU1 MGD MGI:108030
Macaca mulatta HYOU1 VGNC VGNC:73399
Felis catus HYOU1 VGNC VGNC:62861
Bos taurus HYOU1 VGNC VGNC:50032
Others HYOU1 NCBI