1. Gene
  2. NOL3 - nucleolar protein 3 Gene

NOL3 - nucleolar protein 3 Gene

Homo sapiens

Also known as ARC; FCM; MYP; NOP; NOP30; MYOCL1

Gene ID: 8996 | Gene type: protein coding

About NOL3

Cytogenetic location: 16q22.1 Genomic coordinates (GRCh38): 16:67,170,538-67,175,737 (from NCBI)

This gene has 13 transcripts (splice variants), 89 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in skin (RPKM 15.7), prostate (RPKM 15.6) and 24 other tissues.

Summary

This gene encodes an anti-apoptotic protein that has been shown to down-regulate the Enzyme activities of Caspase 2, Caspase 8 and tumor protein p53. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]

NOL3 Products(13)

mRNA Protein Name
NM_001185057.3 NP_001171986.1 nucleolar protein 3 isoform Nop30
NM_001276307.3 NP_001263236.1 nucleolar protein 3 isoform MYP
NM_001276309.3 NP_001263238.1 nucleolar protein 3 isoform MYP
NM_001276311.2 NP_001263240.1 nucleolar protein 3 isoform C
NM_001276312.3 NP_001263241.1 nucleolar protein 3 isoform MYP
NM_001394973.1 NP_001381902.1 nucleolar protein 3 isoform MYP
NM_001394974.1 NP_001381903.1 nucleolar protein 3 isoform C
NM_001394975.1 NP_001381904.1 nucleolar protein 3 isoform C
NM_001394976.1 NP_001381905.1 nucleolar protein 3 isoform C
NM_001394977.1 NP_001381906.1 nucleolar protein 3 isoform Nop30
NM_001394978.1 NP_001381907.1 nucleolar protein 3 isoform Nop30
NM_001394979.1 NP_001381908.1 nucleolar protein 3 isoform E
NM_003946.7 NP_003937.1 nucleolar protein 3 isoform MYP
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables calcium ion binding IMP
IMP: Inferred from mutant phenotype
15509781 GOA
enables caspase binding IPI
IPI: Inferred from physical interaction
9560245 GOA
enables cysteine-type endopeptidase inhibitor activity involved in apoptotic process IDA
IDA: Inferred from direct assay
9560245 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10196175 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
10196175 GOA
located in nucleolus IDA
IDA: Inferred from direct assay
10196175 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

NOL3 Protein Structure

CARD

CARD: Caspase recruitment domain (10 - 95)

  • 0
  • 100
  • 208 a.a.
Protein Preferred Names Protein Names

nucleolar protein 3

muscle-enriched cytoplasmic protein

NOL3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
NOL3 O60936 SPRED1 Homo sapiens Q7Z699 32814053
Intra
NOL3 O60936 SPRED1 Homo sapiens Q7Z699 32814053
Intra
NOL3 O60936 SPRED1 Homo sapiens Q7Z699 32814053
Intra
NOL3 O60936 TINF2 Homo sapiens Q9BSI4 21044950
Intra
NOL3 O60936 ETNK2 Homo sapiens Q9NVF9 16189514
Intra
NOL3 O60936 NOL3 Homo sapiens O60936 16189514
Intra
NOL3 O60936 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
NOL3 O60936 POT1 Homo sapiens Q9NUX5 21044950
Intra
NOL3 O60936 CASP8 Homo sapiens Q14790 18245485
Intra
NOL3 O60936 NIF3L1 Homo sapiens Q9GZT8 16189514
Intra
NOL3 O60936 CASP8 Homo sapiens Q14790 18245485
Intra
NOL3 O60936 NOL3 Homo sapiens O60936 16189514
Intra
NOL3 O60936 SIRPA Homo sapiens P78324 16189514
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant NOL3 Proteins

Cat. No. Product Name Accession Purity
HY-P7540 ARC Protein, Human O60936 (M1-S208) ≥95%

Related Diseases

Diseases Alias
Myoclonus, Familial, 1

Myoclonus, Familial Cortical

MYOCL1

Fcm

Familial Cortical Myoclonus

Myoclonus
Ischemia

Acute Coronary Syndrome

Ulcerative Stomatitis

Stomatitis Ulcerative

Aphthous Stomatitis

Minor Oral Aphthous Ulceration

Familial Adult Myoclonic Epilepsy

Benign Adult Familial Myoclonus Epilepsy

Bafme

Benign Adult Familial Myoclonic Epilepsy

Fame

Familial Cortical Myoclonic Tremor And Epilepsy

Fcmte

Adcme

Autosomal Dominant Cortical Myoclonus And Epilepsy

Fam

Epilepsy, Myoclonic, Familial Adult

Epilepsy, Myoclonic, Benign Adult Familial, Type 2

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
Rattus norvegicus NOL3 RGD RGD:708558
Bos taurus NOL3 VGNC VGNC:32156
Felis catus NOL3 VGNC VGNC:68512
Macaca mulatta NOL3 VGNC VGNC:99529
Mus musculus NOL3 MGD MGI:1925938
Others NOL3 NCBI