1. Gene
  2. PRR7 - proline rich 7, synaptic Gene

PRR7 - proline rich 7, synaptic Gene

Homo sapiens
Gene ID: 80758 | Gene type: protein coding

About PRR7

Cytogenetic location: 5q35.3 Genomic coordinates (GRCh38): 5:177,445,995-177,456,286 (from NCBI)

This gene has 4 transcripts (splice variants), 122 orthologues and 2 paralogues. Biased expression in bone marrow (RPKM 2.0), brain (RPKM 0.9) and 12 other tissues.

Summary

Enables long-chain fatty acid binding activity; protein tyrosine kinase binding activity; and ubiquitin-like protein Ligase binding activity. Involved in negative regulation of protein ubiquitination; positive regulation of apoptotic process; and positive regulation of cysteine-type endopeptidase activity involved in apoptotic signaling pathway. Located in several cellular components, including cytosol; nucleoplasm; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

PRR7 Products(5)

mRNA Protein Name
NM_001174101.2 NP_001167572.1 proline-rich protein 7
NM_001174102.3 NP_001167573.1 proline-rich protein 7
NM_001375593.1 NP_001362522.1 proline-rich protein 7
NM_001375594.1 NP_001362523.1 proline-rich protein 7
NM_030567.5 NP_085044.2 proline-rich protein 7
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables long-chain fatty acid binding IMP
IMP: Inferred from mutant phenotype
21460222 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
27458189 GOA
enables protein tyrosine kinase binding IPI
IPI: Inferred from physical interaction
21460222 GOA
enables ubiquitin-like protein ligase binding IPI
IPI: Inferred from physical interaction
27458189 GOA
Biological Process GO Annotation Evidence Reference Source
involved in positive regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
21460222 GOA
involved in positive regulation of cysteine-type endopeptidase activity involved in apoptotic signaling pathway IMP
IMP: Inferred from mutant phenotype
21460222 GOA
involved in regulation of transcription by RNA polymerase I IMP
IMP: Inferred from mutant phenotype
27458189 GOA
Cellular Component GO Annotation Evidence Reference Source
located in perinuclear region of cytoplasm IMP
IMP: Inferred from mutant phenotype
21460222 GOA
located in plasma membrane IMP
IMP: Inferred from mutant phenotype
21460222 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

PRR7 Protein Structure

WBP-1

WBP-1: WW domain-binding protein 1 (10 - 51)

  • 0
  • 100
  • 200
  • 274 a.a.
Protein Preferred Names Protein Names

proline-rich protein 7

synaptic proline-rich membrane protein

Related Diseases

Diseases Alias
Mitochondrial Complex Ii Deficiency

Isolated Mitochondrial Respiratory Chain Complex Ii Deficiency

Isolated Succinate-Coenzyme Q Reductase Deficiency

Isolated Succinate-Coq Reductase Deficiency

Isolated Succinate-Ubiquinone Reductase Deficiency

Mitochondrial Respiratory Chain Complex Ii Deficiency

Complex 2 Mitochondrial Respiratory Chain Deficiency

Succinate Coq Reductase Deficiency

Succinate Dehydrogenase Deficiency

Isolated Succinate Dehydrogenase Deficiency

Succinate-Coenzyme Q Reductase Deficiency

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
Macaca mulatta PRR7 VGNC VGNC:110441
Canis familiaris PRR7 VGNC VGNC:45049
Mus musculus PRR7 MGD MGI:3487246
Felis catus PRR7 VGNC VGNC:102296
Rattus norvegicus PRR7 RGD RGD:1561898
Bos taurus PRR7 VGNC VGNC:33402