U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SND1-IT1 SND1 intronic transcript 1 [ Homo sapiens (human) ]

Gene ID: 27099, updated on 3-Jul-2022

Summary

Official Symbol
SND1-IT1provided by HGNC
Official Full Name
SND1 intronic transcript 1provided by HGNC
Primary source
HGNC:HGNC:24158
See related
Ensembl:ENSG00000279078 AllianceGenome:HGNC:24158
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
NAG8; NSG-X; C7orf54
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See SND1-IT1 in Genome Data Viewer
Location:
7q32.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (127997509..128000077)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (129309189..129311757)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (127637562..127640130)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene SND1 divergent transcript Neighboring gene staphylococcal nuclease and tudor domain containing 1 Neighboring gene CD2 cytoplasmic tail binding protein 2 pseudogene Neighboring gene uncharacterized LOC124901743 Neighboring gene leucine rich repeat containing 4

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • SND1 intronic transcript 1 (non-protein coding)
  • brain and nasopharyngeal carcinoma susceptibility
  • nasopharyngeal carcinoma associated gene 8

Clone Names

  • MGC138346

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.

RNA

  1. NR_027330.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AF191492, AK024176
    Related
    ENST00000623342.1

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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    127997509..128000077
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    129309189..129311757
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_014411.2: Suppressed sequence

    Description
    NM_014411.2: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.