1. Gene
  2. TUT4 - terminal uridylyl transferase 4 Gene

TUT4 - terminal uridylyl transferase 4 Gene

Homo sapiens

Also known as PAPD3; TENT3A; ZCCHC11

Gene ID: 23318 | Gene type: protein coding

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
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference 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 Reference 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 Reference 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)

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  • 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