1. Gene
  2. RPP21 - ribonuclease P/MRP subunit p21 Gene

RPP21 - ribonuclease P/MRP subunit p21 Gene

Homo sapiens

Also known as CAT60; C6orf135

Gene ID: 79897 | Gene type: protein coding

About RPP21

Cytogenetic location: 6p22.1 Genomic coordinates (GRCh38): 6:30,345,156-30,346,857 (from NCBI)

This gene has 9 transcripts (splice variants), 1 gene allele and 162 orthologues. Ubiquitous expression in endometrium (RPKM 10.7), ovary (RPKM 10.6) and 25 other tissues.

Summary

RPP21 is a protein subunit of nuclear ribonuclease P, which processes the 5-prime leader sequence of precursor tRNAs (Jarrous et al., 2001 [PubMed 11497433]).[supplied by OMIM, Jan 2009]

RPP21 Products(3)

mRNA Protein Name
NM_001199120.3 NP_001186049.1 ribonuclease P protein subunit p21 isoform 1
NM_001199121.3 NP_001186050.1 ribonuclease P protein subunit p21 isoform 3
NM_024839.4 NP_079115.1 ribonuclease P protein subunit p21 isoform 2

RPP21 Protein Structure

Rpr2

Rpr2: RNAse P Rpr2/Rpp21/SNM1 subunit domain (12 - 97)

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

ribonuclease P protein subunit p21

RNaseP protein p21

Related Diseases

Diseases Alias
Anauxetic Dysplasia 2

ANXD2

Anauxetic Dysplasia 1

Anauxetic Dysplasia

Spondylometaepiphyseal Dysplasia, Menger Type

Spondylometaepiphyseal Dysplasia, Anauxetic Type

Spondyloepimetaphyseal Dysplasia, Anauxetic Type

ANXD1

Anxd

Spondylometaepiphyseal Dysplasia Anauxetic Type

Spondylometaepiphyseal Dysplasia Menger Type

Ad

Spondyloepimetaphyseal Dysplasia, Menger Type

Dysplasia, Anauxetic, Type 1

Cartilage-Hair Hypoplasia

Metaphyseal Chondrodysplasia, Mckusick Type

CHH

Mckusick Type Metaphyseal Chondrodysplasia

Metaphyseal Dysplasia Without Hypotrichosis

Cartilage Hair Hypoplasia Like Syndrome

Metaphyseal Chondrodysplasia Mckusick Type

Chhv

Cartilage-Hair Hypoplasia Variant, Skeletal Manifestations Only

Cartilage-Hair Hypoplasia-Like Skeletal Dysplasia Without Hypotrichosis Or Immunodeficiency

Cartilage-Hair Syndrome

Mckusick'S Metaphyseal Chondrodysplasia Syndrome

Metaphyseal Chondrodysplasia, Recessive Type

Autosomal Recessive Metaphyseal Chondrodysplasia

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
Felis catus RPP21 VGNC VGNC:102509
Bos taurus RPP21 VGNC VGNC:106902
Canis familiaris RPP21 VGNC VGNC:54354
Rattus norvegicus RPP21 RGD RGD:1303090
Mus musculus RPP21 MGD MGI:1914926