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C10orf95 chromosome 10 open reading frame 95 [ Homo sapiens (human) ]

Gene ID: 79946, updated on 1-Jun-2020

Summary

Official Symbol
C10orf95provided by HGNC
Official Full Name
chromosome 10 open reading frame 95provided by HGNC
Primary source
HGNC:HGNC:25880
See related
Ensembl:ENSG00000120055
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 lung (RPKM 2.4), thyroid (RPKM 2.2) and 25 other tissues See more
Orthologs

Genomic context

See C10orf95 in Genome Data Viewer
Location:
10q24.32
Exon count:
2
Annotation release Status Assembly Chr Location
109.20200522 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (102449837..102451543, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (104209594..104211300, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene CUE domain containing 2 Neighboring gene microRNA 146b Neighboring gene RPARP antisense RNA 1 Neighboring gene major facilitator superfamily domain containing 13A Neighboring gene actin related protein 1A Neighboring gene SUFU negative regulator of hedgehog signaling Neighboring gene ribosomal protein L23a pseudogene 58

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

Phenotypes

NHGRI GWAS Catalog

Description
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
NHGRI GWA Catalog

General protein information

Preferred Names
uncharacterized protein C10orf95

NCBI Reference Sequences (RefSeq)

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_001363580.1NP_001350509.1  uncharacterized protein C10orf95

    Status: VALIDATED

    Source sequence(s)
    AK024342, AL121928
    Related
    ENSP00000489684.1, ENST00000625129.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    102449837..102451543 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_024886.2: Suppressed sequence

    Description
    NM_024886.2: This RefSeq was removed because currently it is thought that it is annotated with an incorrect coding sequence.
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