1. Gene
  2. NIP7 - nucleolar pre-rRNA processing protein NIP7 Gene

NIP7 - nucleolar pre-rRNA processing protein NIP7 Gene

Homo sapiens

Also known as KD93; CGI-37; HSPC031

Gene ID: 51388 | Gene type: protein coding

About NIP7

Cytogenetic location: 16q22.1 Genomic coordinates (GRCh38): 16:69,339,772-69,343,106 (from NCBI)

This gene has 8 transcripts (splice variants), 223 orthologues and 2 paralogues. Ubiquitous expression in lymph node (RPKM 9.5), appendix (RPKM 8.7) and 25 other tissues.

Summary

Enables RNA binding activity. Predicted to be involved in ribosomal large subunit biogenesis. Located in cytosol; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

NIP7 Products(2)

mRNA Protein Name
NM_001199434.2 NP_001186363.1 60S ribosome subunit biogenesis protein NIP7 homolog isoform 2
NM_016101.5 NP_057185.1 60S ribosome subunit biogenesis protein NIP7 homolog isoform 1
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
14660641 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

NIP7 Protein Structure

UPF0113

UPF0113: Uncharacterised protein family (UPF0113) (2 - 175)

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

60S ribosome subunit biogenesis protein NIP7 homolog

NIP7, nucleolar pre-rRNA processing protein

Recombinant NIP7 Proteins

Cat. No. Product Name Accession Purity
HY-P71162 NIP7 Protein, Human (His) Q9Y221-1 (M1-T180) ≥95%

Related Diseases

Diseases Alias
Shwachman-Diamond Syndrome 1

Shwachman-Diamond Syndrome

Shwachman Syndrome

Shwachman-Bodian-Diamond Syndrome

Sds

Pancreatic Insufficiency And Bone Marrow Dysfunction

Shwachman-Bodian Syndrome

SDS1

Lipomatosis Of Pancreas, Congenital

Congenital Lipomatosis Of Pancreas

Shwachman-Diamond Type Metaphyseal Dysplasia

Metaphyseal Chondrodysplasia, Shwachman Type

Shwachman-Diamond-Oski 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
Bos taurus NIP7 VGNC VGNC:32080
Mus musculus NIP7 MGD MGI:1913414
Felis catus NIP7 VGNC VGNC:63806
Canis familiaris NIP7 VGNC VGNC:43814
Rattus norvegicus NIP7 RGD RGD:620069
Macaca mulatta NIP7 VGNC VGNC:99527
Others NIP7 NCBI