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C16orf46 chromosome 16 open reading frame 46 [ Homo sapiens (human) ]

Gene ID: 123775, updated on 5-Mar-2024

Summary

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Official Symbol
C16orf46provided by HGNC
Official Full Name
chromosome 16 open reading frame 46provided by HGNC
Primary source
HGNC:HGNC:26525
See related
Ensembl:ENSG00000166455 AllianceGenome:HGNC:26525
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
Summary
Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]
Expression
Broad expression in testis (RPKM 4.0), thyroid (RPKM 3.1) and 18 other tissues See more
Orthologs
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Genomic context

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See C16orf46 in Genome Data Viewer
Location:
16q23.2
Exon count:
7
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (81053497..81077238, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (87115033..87138779, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (81087102..81110843, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11174 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11175 Neighboring gene CENPN antisense RNA 1 Neighboring gene centromere protein N Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 7749 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 7750 Neighboring gene ATM interactor Neighboring gene uncharacterized LOC105371361 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11176 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:81110606-81111266 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:81111267-81111925 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 7751 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 7752 Neighboring gene glycine cleavage system protein H Neighboring gene RNA, U6 small nuclear 1191, pseudogene Neighboring gene polycystin 1 like 2 (gene/pseudogene)

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: 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

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Related articles in PubMed

  1. Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. Anney RJ, et al. Am J Med Genet B Neuropsychiatr Genet, 2008 Dec 5. PMID 18951430
  2. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. Rose JE, et al. Mol Med, 2010 Jul-Aug. PMID 20379614, Free PMC Article
  3. Toward a confocal subcellular atlas of the human proteome. Barbe L, et al. Mol Cell Proteomics, 2008 Mar. PMID 18029348
  4. Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei. Fasci D, et al. Mol Cell Proteomics, 2018 Oct. PMID 30021884, Free PMC Article
  5. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560, Free PMC Article

See all (9) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
    Title: Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Submit: New GeneRIF Correction

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

EBI GWAS Catalog

Description
Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Clone Names

  • FLJ32702

Gene Ontology Provided by GOA

Component Evidence Code Pubs
located_in cytosol IDA
Inferred from Direct Assay
more info
  
located_in nucleoplasm IDA
Inferred from Direct Assay
more info
  

General protein information

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Preferred Names
uncharacterized protein C16orf46

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_001100873.2 → NP_001094343.1  uncharacterized protein C16orf46 isoform 1

    See identical proteins and their annotated locations for NP_001094343.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) encodes the longer isoform (1).
    Source sequence(s)
    AC092718, AK057264, BC064143, DA525473
    Consensus CDS
    CCDS42201.1
    UniProtKB/Swiss-Prot
    Q6P387
    Related
    ENSP00000367874.4, ENST00000378611.8
    Conserved Domains (1) summary
    pfam15032
    Location:1 → 381
    DUF4529; Protein of unknown function (DUF4529)

  2. NM_152337.3 → NP_689550.2  uncharacterized protein C16orf46 isoform 2

    See identical proteins and their annotated locations for NP_689550.2

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks differs in the 5' UTR and in the 3' UTR and coding region compared to variant 1. The resulting isoform (2) has a shorter and distinct C-terminus compared to isoform 1.
    Source sequence(s)
    AA905107, AC092718, AK057264, BC064143, DA525473
    Consensus CDS
    CCDS10932.1
    UniProtKB/Swiss-Prot
    Q6P387, Q96MA7
    Related
    ENSP00000299578.4, ENST00000299578.10
    Conserved Domains (1) summary
    pfam15032
    Location:1 → 395
    DUF4529; Protein of unknown function (DUF4529)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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
    81053497..81077238 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_005255792.3 → XP_005255849.1  uncharacterized protein C16orf46 isoform X2

    See identical proteins and their annotated locations for XP_005255849.1

    UniProtKB/Swiss-Prot
    Q6P387
    Conserved Domains (1) summary
    pfam15032
    Location:1 → 381
    DUF4529; Protein of unknown function (DUF4529)

  2. XM_047433586.1 → XP_047289542.1  uncharacterized protein C16orf46 isoform X1

    UniProtKB/Swiss-Prot
    Q6P387, Q96MA7

  3. XM_011522849.3 → XP_011521151.3  uncharacterized protein C16orf46 isoform X1

    UniProtKB/Swiss-Prot
    Q6P387, Q96MA7

  4. XM_011522848.3 → XP_011521150.3  uncharacterized protein C16orf46 isoform X1

    UniProtKB/Swiss-Prot
    Q6P387, Q96MA7

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_025791800.1 Reference GRCh38.p14 PATCHES

    Range
    101736..125477 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054333190.1 → XP_054189165.1  uncharacterized protein C16orf46 isoform X2

  2. XM_054333189.1 → XP_054189164.1  uncharacterized protein C16orf46 isoform X1

    UniProtKB/Swiss-Prot
    Q6P387, Q96MA7

  3. XM_054333187.1 → XP_054189162.1  uncharacterized protein C16orf46 isoform X1

    UniProtKB/Swiss-Prot
    Q6P387, Q96MA7

  4. XM_054333188.1 → XP_054189163.1  uncharacterized protein C16orf46 isoform X1

    UniProtKB/Swiss-Prot
    Q6P387, Q96MA7

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    87115033..87138779 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054379540.1 → XP_054235515.1  uncharacterized protein C16orf46 isoform X2

  2. XM_054379539.1 → XP_054235514.1  uncharacterized protein C16orf46 isoform X1

  3. XM_054379537.1 → XP_054235512.1  uncharacterized protein C16orf46 isoform X1

  4. XM_054379538.1 → XP_054235513.1  uncharacterized protein C16orf46 isoform X1

Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q6P387.2 GenPept UniProtKB/Swiss-Prot:Q6P387

Gene LinkOut

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