PNO1 - partner of NOB1 homolog Gene

Also Known as RRP20; KHRBP1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 56902

About PNO1

Cytogenetic location: 2p14 Genomic coordinates (GRCh38): 2:68,157,888-68,176,238 (from NCBI)

This gene has 3 transcripts (splice variants) and 220 orthologues. Ubiquitous expression in thyroid (RPKM 8.8), adrenal (RPKM 8.5) and 25 other tissues.

Summary

Enables RNA binding activity. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

PNO1 Products (3)

mRNA Protein Name
NM_001329916.2 NP_001316845.1 RNA-binding protein PNO1 isoform 2
NM_001329917.2 NP_001316846.1 RNA-binding protein PNO1 isoform 3
NM_020143.4 NP_064528.1 RNA-binding protein PNO1 isoform 1
Molecular Function GO Annotation Evidence Verweise Source
enables protein binding IPI
IPI: Inferred from physical interaction
28514442 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in ribosomal small subunit biogenesis IDA
IDA: Inferred from direct assay
34516797 GOA
Cellular Component GO Annotation Evidence Verweise Source
located in nucleolus IDA
IDA: Inferred from direct assay
15497447 GOA
part of small-subunit processome IDA
IDA: Inferred from direct assay
34516797 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

PNO1 Protein Structure

KH_1

KH_1: KH domain (178 - 225)

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

RNA-binding protein PNO1

  • KH-type RNA-binding protein 1

PNO1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
PNO1 Q9NRX1 JPH3 Homo sapiens Q8WXH2 32814053
Intra
PNO1 Q9NRX1 JPH3 Homo sapiens Q8WXH2 32814053
Intra
PNO1 Q9NRX1 JPH3 Homo sapiens Q8WXH2 32814053
Intra
PNO1 Q9NRX1 NOB1 Homo sapiens Q9ULX3 33961781
Intra
PNO1 Q9NRX1 NOB1 Homo sapiens Q9ULX3 32296183
Intra
PNO1 Q9NRX1 NOB1 Homo sapiens Q9ULX3 32296183
Intra
PNO1 Q9NRX1 NOB1 Homo sapiens Q9ULX3 28514442
Intra
PNO1 Q9NRX1 NOB1 Homo sapiens Q9ULX3 32296183
Intra
PNO1 Q9NRX1 PICK1 Homo sapiens Q9NRD5 32296183
Intra
PNO1 Q9NRX1 PICK1 Homo sapiens Q9NRD5 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hermansky-Pudlak Syndrome 3
  • HPS3

  • Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial

  • Delta Storage Pool Disease

  • Hermansky-Pudlak Syndrome, Type 3

  • Platelet Storage Pool Deficiency

  • Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

Diamond-Blackfan Anemia
  • Congenital Pure Red Cell Aplasia

  • Aase Syndrome

  • Erythrogenesis Imperfecta

  • Anemia, Diamond-Blackfan

  • Congenital Hypoplastic Anemia

  • Aase-Smith Ii Syndrome

  • Bds

  • Blackfan-Diamond Anemia

  • Congenital Prca

  • Congenital Hypoplastic Anemia, Blackfan-Diamond Type

  • Dba

  • Blackfan - Diamond Syndrome

  • Chronic Constitutional Pure Red Cell Anaemia

  • Anemia Diamond Blackfan Type

  • Anemia Congenital Erythroid Hypoplastic

  • Aregenerative Anemia Chronic Congenital

  • Blackfan Diamond Syndrome

  • Red Cell Aplasia, Pure Hereditary

  • Aase-Smith Syndrome Ii

  • Bda

  • Blackfan Diamond Anemia

  • Blackfan-Diamond Disease

  • Blackfan-Diamond Syndrome

  • Chronic Congenital Agenerative Anemia

  • Congenital Erythroid Hypoplastic Anemia

  • Congenital Hypoplastic Anemia Of Blackfan And Diamond

  • Congenital Pure Red Cell Anemia

  • Hypoplastic Congenital Anemia

  • Inherited Erythroblastopenia

  • Pure Hereditary Red Cell Aplasia

  • Anemia, Hypoplastic, Congenital

  • Anemia Hypoplastic Congenital

  • Fanconi Anemia

  • Constitutional Aplastic Anemia

  • Diamond-Blackfan Anemia 1

  • Aase Smith Syndrome 2

  • Congenital Red Cell Aplasia

  • Red Cell Aplasia Of Infants

  • Pure Red Cell Aplasia Of Infants

  • Congenital Red Cell Aplastic Anaemia

  • Congenital Pure Red Cell Anaemia

  • Congenital Erythroid Hypoplasia

  • Pearson Marrow-Pancreas 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
Mus musculus PNO1 MGD MGI:1913499
Canis familiaris PNO1 VGNC VGNC:44749
Bos taurus PNO1 VGNC VGNC:33088
Rattus norvegicus PNO1 RGD RGD:727882
Others PNO1 NCBI