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C10orf126 chromosome 10 open reading frame 126 [ Homo sapiens (human) ]

Gene ID: 283080, updated on 13-May-2022

Summary

Official Symbol
C10orf126provided by HGNC
Official Full Name
chromosome 10 open reading frame 126provided by HGNC
Primary source
HGNC:HGNC:28693
See related
Ensembl:ENSG00000232624 AllianceGenome:HGNC:28693
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
bA492M23.1
Expression
Low expression observed in reference dataset See more
Orthologs
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Genomic context

See C10orf126 in Genome Data Viewer
Location:
10p12.1
Exon count:
5
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (28846408..28881898)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (28878333..28913800)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (29135337..29170827)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1517 Neighboring gene RNA, U6 small nuclear 270, pseudogene Neighboring gene long intergenic non-protein coding RNA 837 Neighboring gene heart enhancer 23 Neighboring gene RNA, 5S ribosomal pseudogene 308 Neighboring gene ribosomal protein L21 pseudogene 93 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:29279785-29280984

Genomic regions, transcripts, and products

Expression

  • 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

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.

RNA

  1. NR_164114.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL390248
    Related
    ENST00000375520.4

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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    28846408..28881898
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    28878333..28913800
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001278522.1: Suppressed sequence

    Description
    NM_001278522.1: This RefSeq was removed because it is now thought that this gene does not encode a protein.
  2. NM_173577.1: Suppressed sequence

    Description
    NM_173577.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.