TUT4 - terminal uridylyl transferase 4 Gene

Also Known as PAPD3; TENT3A; ZCCHC11

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 23318

About TUT4

Cytogenetic location: 1p32.3 Genomic coordinates (GRCh38): 1:52,423,275-52,553,463 (from NCBI)

This gene has 21 transcripts (splice variants), 257 orthologues and 4 paralogues. Ubiquitous expression in testis (RPKM 11.1), thyroid (RPKM 9.7) and 25 other tissues.

Summary

ZCCHC11 is an RNA uridyltransferase (EC 2.7.7.52) that uses UTP to add uridines to the 3-prime end of substrate RNA molecules (Jones et al., 2009 [PubMed 19701194]).[supplied by OMIM, Jan 2011]

TUT4 Products (2)

mRNA Protein Name
NM_001009881.3 NP_001009881.1 terminal uridylyltransferase 4 isoform a
NM_015269.2 NP_056084.1 terminal uridylyltransferase 4 isoform b
Molecular Function GO Annotation Evidence References Source
enables RNA uridylyltransferase activity IDA
IDA: Inferred from direct assay
19703396 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16643855 GOA
Biological Process GO Annotation Evidence References Source
involved in RNA 3'-end processing IDA
IDA: Inferred from direct assay
19703396 GOA
NOT involved in histone mRNA catabolic process IMP
IMP: Inferred from mutant phenotype
18172165 GOA
involved in miRNA catabolic process IMP
IMP: Inferred from mutant phenotype
19703396 GOA
involved in miRNA metabolic process IDA
IDA: Inferred from direct assay
25979828 GOA
involved in pre-miRNA processing IDA
IDA: Inferred from direct assay
25979828 GOA
involved in pre-miRNA processing IMP
IMP: Inferred from mutant phenotype
19703396 GOA
involved in retrotransposon silencing by mRNA destabilization IDA
IDA: Inferred from direct assay
30122351 GOA
involved in stem cell population maintenance IMP
IMP: Inferred from mutant phenotype
19703396 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
19703396 GOA
located in cytoplasmic ribonucleoprotein granule IDA
IDA: Inferred from direct assay
30122351 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

TUT4 Protein Structure

PAP_assoc

PAP_assoc: Cid1 family poly A polymerase (628 - 678)

NTP_transf_2

NTP_transf_2: Nucleotidyltransferase domain (981 - 1052)

PAP_assoc

PAP_assoc: Cid1 family poly A polymerase (1184 - 1237)

zf-CCHC

zf-CCHC: Zinc knuckle (1293 - 1310)

zf-CCHC

zf-CCHC: Zinc knuckle (1358 - 1374)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1500
  • 1644 a.a.
Protein Preferred Names Protein Names

terminal uridylyltransferase 4

  • PAP associated domain containing 3

Related Diseases

Diseases Alias
Perlman Syndrome
  • Nephroblastomatosis, Fetal Ascites, Macrosomia And Wilms Tumor

  • PRLMNS

  • Renal Hamartomas, Nephroblastomatosis, And Fetal Gigantism

  • Nephroblastomatosis Fetal Ascites Macrosomia And Wilms Tumor

  • Nephroblastomatosis, Fetal Ascites, Macrosomia, And Wilms Tumor

  • Nephroblastomatosis - Fetal Ascites - Macrosomia - Wilms Tumor

  • Renal Hamartomas, Nephroblastomatosis And Fetal Gigantism

  • Nephroblastomatosis-Fetal Ascites-Macrosomia-Wilms Tumor Syndrome

  • Renal Hamartomas Nephroblastomatosis And Fetal Gigantism

  • Nephroblastoma

  • Fetal Macrosomia

Trichothiodystrophy 1, Photosensitive
  • TTD1

  • Tay Syndrome

  • Trichothiodystrophy With Congenital Ichthyosis

  • Photosensitive Trichothiodystrophy

  • Ibids Syndrome

  • Ttdp

  • Ichthyosiform Erythroderma With Hair Abnormality And Mental And Growth Retardation

  • Ichthyosis, Congenital, With Trichothiodystrophy

  • Pibids Syndrome

  • Photosensitive Trichothiodystrophy 1

  • Trichothiodystrophy, Photosensitive

  • Sulfur-Deficient Brittle Hair Syndrome

  • Ttd-P

  • Ichthyosis With Brittle Hair, Intellectual Impairment, Decreased Fertility And Short Stature

  • Trichothiodystrophy Photosensitive

  • Trichothiodystrophy, Type 1

  • Tricho-Thiodystrophy Disorder

  • Trichothiodystrophy Syndromes

  • Amish Brittle Hair Brain Syndrome

Trichothiodystrophy 6, Nonphotosensitive
  • TTD6

  • Nonphotosensitive Trichothiodystrophy 6

  • Trichothiodystrophy 6, Non-Photosensitive

Renal Wilms' Tumor
  • Nonanaplastic Renal Wilm'S Tumor

  • Nonanaplastic Renal Wilm'S Tumour

  • Nonanaplastic Renal Wilms Tumor

  • Renal Wilms' Tumour

Nonphotosensitive Trichothiodystrophy
  • Trichothiodystrophy Nonphotosensitive

  • Amish Brittle Hair Brain Syndrome

Spastic Ataxia 4
Wilms Tumor 1
  • Nephroblastoma

  • Wilms Tumor

  • WT1

  • Wilms' Tumor

  • Bilateral Wilms Tumor

  • Wilms Tumor, Type 1

  • Wilms Tumor, Somatic

  • Adult Nephroblastoma

  • Wt1 Disorder

  • Renal Embryonic Tumor

  • Adult Kidney Wilms Tumor

  • Childhood Kidney Wilms Tumor

  • Nonanaplastic Kidney Wilms Tumor

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
Canis familiaris TUT4 VGNC VGNC:48566
Bos taurus TUT4 VGNC VGNC:37116
Felis catus TUT4 VGNC VGNC:66714
Mus musculus TUT4 MGD MGI:2445126
Macaca mulatta TUT4 VGNC VGNC:79759
Rattus norvegicus TUT4 RGD RGD:1310138
Others TUT4 NCBI