1. Gene
  2. TRUB1 - TruB pseudouridine synthase family member 1 Gene

TRUB1 - TruB pseudouridine synthase family member 1 Gene

Homo sapiens

Also known as PUS4

Gene ID: 142940 | Gene type: protein coding

About TRUB1

Cytogenetic location: 10q25.3 Genomic coordinates (GRCh38): 10:114,938,195-114,977,676 (from NCBI)

This gene has 2 transcripts (splice variants) and 194 orthologues. Ubiquitous expression in adrenal (RPKM 19.3), testis (RPKM 13.5) and 24 other tissues.

Summary

Pseudouridine is an abundant component of rRNAs and tRNAs and is enzymatically generated by isomerization of uridine by pseudouridine synthase (Zucchini et al., 2003 [PubMed 12736709]).[supplied by OMIM, Mar 2008]

TRUB1 Products(1)

mRNA Protein Name
NM_139169.5 NP_631908.1 pseudouridylate synthase TRUB1

TRUB1 Protein Structure

TruB_N

TruB_N: TruB family pseudouridylate synthase (N terminal domain) (106 - 255)

  • 0
  • 100
  • 200
  • 300
  • 349 a.a.
Protein Preferred Names Protein Names

pseudouridylate synthase TRUB1

TruB pseudouridine (psi) synthase family member 1

Related Diseases

Diseases Alias
Dyskeratosis Congenita

Dyskeratosis Congenita Autosomal Dominant

Dc

Dkc

Zinsser-Engman-Cole Syndrome

Dyskeratosis Congenita, Autosomal Dominant

Autosomal Dominant Dyskeratosis Congenita

Dkca

Dyskeratosis Congenita Scoggins Type

Zinsser-Cole-Engman Syndrome

X-Linked Dyskeratosis Congenita

Hoyeraal-Hreidarsson Syndrome

Myopathy, Lactic Acidosis, And Sideroblastic Anemia 1

Mitochondrial Myopathy And Sideroblastic Anemia

MLASA1

Mlasa

Myopathy, Lactic Acidosis And Sideroblastic Anemia

Myopathy With Lactic Acidosis And Sideroblastic Anemia

Sideroblastic Anemia And Mitochondrial Myopathy

Myopathy With Lactic Acidosis And Sideroblastic Anemia 1

Dyskeratosis Congenita, X-Linked

DKCX

X-Linked Dyskeratosis Congenita

Zinsser-Cole-Engman Syndrome

Hoyeraal-Hreidarsson Syndrome

Dyskeratosis Congenita X-Linked

HHS

Cerebellar Hypoplasia With Pancytopenia

Prenatal Growth Retardation With Progressive Pancytopenia And Cerebellar Hypoplasia

Dyskeratosis Congenita

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 TRUB1 VGNC VGNC:36404
Felis catus TRUB1 VGNC VGNC:66602
Mus musculus TRUB1 MGD MGI:1919383
Canis familiaris TRUB1 VGNC VGNC:47888
Macaca mulatta TRUB1 VGNC VGNC:79005
Rattus norvegicus TRUB1 RGD RGD:1308502