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    TENT5C terminal nucleotidyltransferase 5C [ Homo sapiens (human) ]

    Gene ID: 54855, updated on 2-Nov-2024

    Summary

    Official Symbol
    TENT5Cprovided by HGNC
    Official Full Name
    terminal nucleotidyltransferase 5Cprovided by HGNC
    Primary source
    HGNC:HGNC:24712
    See related
    Ensembl:ENSG00000183508 MIM:613952; AllianceGenome:HGNC:24712
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    FAM46C
    Summary
    Enables poly(A) RNA polymerase activity. Involved in mRNA stabilization and negative regulation of cell differentiation. Located in centrosome; cytoplasm; and nucleoplasm. [provided by Alliance of Genome Resources, Nov 2024]
    Expression
    Broad expression in bone marrow (RPKM 37.0), testis (RPKM 24.1) and 20 other tissues See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See TENT5C in Genome Data Viewer
    Location:
    1p12
    Exon count:
    2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (117606048..117628389)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (117615263..117637599)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (118148670..118171011)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene VPS25 pseudogene 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:118105543-118105787 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1582 Neighboring gene TENT5C divergent transcript Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:118147484-118147984 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:118147985-118148485 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:118172930-118173480 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:118173481-118174031 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1243 Neighboring gene VDAC2 pseudogene 3 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1583 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1584 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1585 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1586 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1587 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1588 Neighboring gene small nucleolar RNA SNORA40

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Potential readthrough

    Included gene: WDR3

    Clone Names

    • FLJ20202

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables RNA binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables poly(A) RNA polymerase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables poly(A) RNA polymerase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in in utero embryonic development IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in mRNA stabilization IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in mRNA stabilization IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in negative regulation of cell differentiation IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in centrosome IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
     
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    terminal nucleotidyltransferase 5C
    Names
    family with sequence similarity 46 member C
    non-canonical poly(A) polymerase FAM46C
    protein FAM46C
    putative nucleotidyltransferase FAM46C
    NP_060179.2

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_017709.4NP_060179.2  terminal nucleotidyltransferase 5C

      See identical proteins and their annotated locations for NP_060179.2

      Status: VALIDATED

      Source sequence(s)
      AL365331, BC036516, CD300120
      Consensus CDS
      CCDS896.1
      UniProtKB/Swiss-Prot
      A3KMG2, Q5VWP2, Q8NE25, Q9NXK0
      Related
      ENSP00000358458.3, ENST00000369448.4
      Conserved Domains (1) summary
      pfam07984
      Location:17334
      NTP_transf_7; Nucleotidyltransferase

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      117606048..117628389
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      117615263..117637599
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)