1. Gene
  2. UTP14A - UTP14A small subunit processome component Gene

UTP14A - UTP14A small subunit processome component Gene

Homo sapiens

Also known as Utp14; NYCO16; SDCCAG16; dJ537K23.3

Gene ID: 10813 | Gene type: protein coding

About UTP14A

Cytogenetic location: Xq26.1 Genomic coordinates (GRCh38): X:129,906,164-129,929,752 (from NCBI)

This gene has 4 transcripts (splice variants), 230 orthologues and 1 paralogue. Ubiquitous expression in lymph node (RPKM 5.9), appendix (RPKM 5.8) and 25 other tissues.

Summary

This gene encodes a member of the uridine triphosphate 14 family. As an essential component of a large ribonucleoprotein complex bound to the U3 small nucleolar RNA, the encoded protein is involved in ribosome biogenesis and 18S rRNA synthesis. An autosomal retrotransposed copy of this X-linked gene exists on chromosome 13. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]

UTP14A Products(2)

mRNA Protein Name
NM_001166221.2 NP_001159693.1 U3 small nucleolar RNA-associated protein 14 homolog A isoform 2
NM_006649.4 NP_006640.2 U3 small nucleolar RNA-associated protein 14 homolog A isoform 1

UTP14A Protein Structure

Utp14

Utp14: Utp14 protein (31 - 735)

  • 0
  • 200
  • 400
  • 600
  • 771 a.a.
Protein Preferred Names Protein Names

U3 small nucleolar RNA-associated protein 14 homolog A

UTP14, U3 small nucleolar ribonucleoprotein, homolog A

UTP14A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
UTP14A Q9BVJ6 JPH3 Homo sapiens Q8WXH2 32814053
Intra
UTP14A Q9BVJ6 JPH3 Homo sapiens Q8WXH2 32814053
Intra
UTP14A Q9BVJ6 JPH3 Homo sapiens Q8WXH2 32814053
Intra
UTP14A Q9BVJ6 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
UTP14A Q9BVJ6 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
UTP14A Q9BVJ6 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
UTP14A Q9BVJ6 APLP2 Homo sapiens Q06481-5 32814053
Intra
UTP14A Q9BVJ6 APLP2 Homo sapiens Q06481-5 32814053
Intra
UTP14A Q9BVJ6 APLP2 Homo sapiens Q06481-5 32814053
Intra
UTP14A Q9BVJ6 GADD45G Homo sapiens O95257
Y2H
15383276
Intra
UTP14A Q9BVJ6 GADD45G Homo sapiens O95257
Y2H
21900206
Intra
UTP14A Q9BVJ6 A2M Homo sapiens P01023 32814053
Intra
UTP14A Q9BVJ6 A2M Homo sapiens P01023 32814053
Intra
UTP14A Q9BVJ6 A2M Homo sapiens P01023 32814053
Intra
UTP14A Q9BVJ6 ATXN10 Homo sapiens Q9UBB4 32814053
Intra
UTP14A Q9BVJ6 ATXN10 Homo sapiens Q9UBB4 32814053
Intra
UTP14A Q9BVJ6 ATXN10 Homo sapiens Q9UBB4 32814053
Intra
UTP14A Q9BVJ6 BLMH Homo sapiens Q13867 32814053
Intra
UTP14A Q9BVJ6 BLMH Homo sapiens Q13867 32814053
Intra
UTP14A Q9BVJ6 BLMH Homo sapiens Q13867 32814053
Intra
UTP14A Q9BVJ6 LDOC1 Homo sapiens O95751 16189514
Intra
UTP14A Q9BVJ6 LDOC1 Homo sapiens O95751 31515488
Intra
UTP14A Q9BVJ6 SMYD1 Homo sapiens Q8NB12
Y2H
23455924
Intra
UTP14A Q9BVJ6 CSNK1D Homo sapiens P48730-2 32814053
Intra
UTP14A Q9BVJ6 CSNK1D Homo sapiens P48730-2 32814053
Intra
UTP14A Q9BVJ6 CSNK1D Homo sapiens P48730-2 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Bowen-Conradi Syndrome

BWCNS

Bowen Hutterite Syndrome

Bowen-Conradi Hutterite Syndrome

Bowen Syndrome, Hutterite Type

Bowen Hutterite Syndrome, Formerly

Hutterite Syndrome

Bowen Syndrome Hutterite Type

Fetal Growth Retardation

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 UTP14A RGD RGD:1359313
Mus musculus UTP14A MGD MGI:1919804
Macaca mulatta UTP14A VGNC VGNC:103882