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    C1orf226 chromosome 1 open reading frame 226 [ Homo sapiens (human) ]

    Gene ID: 400793, updated on 19-Dec-2024

    Summary

    Official Symbol
    C1orf226provided by HGNC
    Official Full Name
    chromosome 1 open reading frame 226provided by HGNC
    Primary source
    HGNC:HGNC:34351
    See related
    Ensembl:ENSG00000239887 AllianceGenome:HGNC:34351
    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
    Expression
    Ubiquitous expression in colon (RPKM 4.5), adrenal (RPKM 4.4) and 23 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See C1orf226 in Genome Data Viewer
    Location:
    1q23.3
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (162378841..162386812)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (161722817..161730827)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (162348631..162356602)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene nitric oxide synthase 1 adaptor protein Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:162324648-162325148 Neighboring gene ReSE screen-validated silencer GRCh37_chr1:162327537-162327759 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:162336993-162337492 Neighboring gene microRNA 556 Neighboring gene Sharpr-MPRA regulatory region 12682 Neighboring gene Sharpr-MPRA regulatory region 4437 Neighboring gene spermatogenesis associated 46 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:162389320-162390519 Neighboring gene SH2 domain containing 1B Neighboring gene SLAM family member 6 pseudogene 1

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Potential readthrough

    Included gene: NOS1AP

    Clone Names

    • FLJ13137, FLJ43132, FLJ55152

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 

    General protein information

    Preferred Names
    uncharacterized protein C1orf226

    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_001085375.2NP_001078844.1  uncharacterized protein C1orf226

      See identical proteins and their annotated locations for NP_001078844.1

      Status: VALIDATED

      Source sequence(s)
      AI480219, AK125122, AL512785
      Consensus CDS
      CCDS53422.1
      UniProtKB/Swiss-Prot
      A1L170, B4DF31
      Related
      ENSP00000437071.1, ENST00000458626.4
      Conserved Domains (1) summary
      pfam15429
      Location:1272
      DUF4628; Domain of unknown function (DUF4628)
    2. NM_001135240.4NP_001128712.2  uncharacterized protein C1orf226

      Status: VALIDATED

      Source sequence(s)
      AL512785
      Consensus CDS
      CCDS44268.1
      Related
      ENSP00000413150.2, ENST00000426197.2

    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
      162378841..162386812
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      161722817..161730827
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)