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C16orf82 chromosome 16 open reading frame 82 [ Homo sapiens (human) ]

Gene ID: 162083, updated on 13-Aug-2022

Summary

Official Symbol
C16orf82provided by HGNC
Official Full Name
chromosome 16 open reading frame 82provided by HGNC
Primary source
HGNC:HGNC:30755
See related
Ensembl:ENSG00000234186 AllianceGenome:HGNC:30755
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
TNT
Orthologs
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Genomic context

See C16orf82 in Genome Data Viewer
Location:
16p12.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (27066927..27069166)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (27343670..27345909)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (27078248..27080487)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105371153 Neighboring gene uncharacterized LOC105371154 Neighboring gene eukaryotic translation elongation factor 1 alpha 1 pseudogene 38 Neighboring gene uncharacterized LOC105371155

Genomic regions, transcripts, and products

General gene information

Markers

Homology

Clone Names

  • FLJ18616

NCBI Reference Sequences (RefSeq)

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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_001145545.2NP_001139017.1  protein TNT

    Status: VALIDATED

    Source sequence(s)
    AC092725
    UniProtKB/Swiss-Prot
    Q7Z2V1
    UniProtKB/TrEMBL
    A0A5F9ZHF3
    Related
    ENSP00000500329.2, ENST00000505035.3
    Conserved Domains (1) summary
    pfam15765
    Location:1153
    DUF4694; Domain of unknown function (DUF4694)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    27066927..27069166
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    27343670..27345909
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_182831.1: Suppressed sequence

    Description
    NM_182831.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.