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C8orf17 chromosome 8 putative open reading frame 17 [ Homo sapiens (human) ]

Gene ID: 100507249, updated on 13-May-2022

Summary

Official Symbol
C8orf17provided by HGNC
Official Full Name
chromosome 8 putative open reading frame 17provided by HGNC
Primary source
HGNC:HGNC:17737
See related
Ensembl:ENSG00000250733 MIM:616992; AllianceGenome:HGNC:17737
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
MOST1; MOST-1
Summary
Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See C8orf17 in Genome Data Viewer
Location:
8q24.3
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (139931420..139933944)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (141051303..141053826)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (140943664..140946188)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene trafficking protein particle complex subunit 9 Neighboring gene uncharacterized LOC107986981 Neighboring gene uncharacterized LOC105375781 Neighboring gene glyceraldehyde-3-phosphate dehydrogenase pseudogene Neighboring gene paternally expressed 13

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

General gene information

Other Names

  • MOLT-4 T-cell lymphoblastic leukemia sequence tag-1
  • MOLT-4 sequence tag-1

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Component Evidence Code Pubs
located_in cytoplasm IDA
Inferred from Direct Assay
more info
PubMed 
located_in endoplasmic reticulum membrane IEA
Inferred from Electronic Annotation
more info
 
located_in nucleus IDA
Inferred from Direct Assay
more info
PubMed 

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_172942.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC021744
    Related
    ENST00000507535.4

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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    139931420..139933944
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    141051303..141053826
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_020237.1: Suppressed sequence

    Description
    NM_020237.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.