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ELFN1-AS1 ELFN1 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 101927125, updated on 23-Nov-2021

Summary

Official Symbol
ELFN1-AS1provided by HGNC
Official Full Name
ELFN1 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:39071
See related
Ensembl:ENSG00000236081
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
MYCLo-2
Expression
Low expression observed in reference dataset See more
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Genomic context

See ELFN1-AS1 in Genome Data Viewer
Location:
7p22.3
Exon count:
2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 7 NC_000007.14 (1738630..1742310, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (1778266..1781946, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375124 Neighboring gene extracellular leucine rich repeat and fibronectin type III domain containing 1 Neighboring gene lncRNA radiation induced regulator of PLK1 and RAD51 Neighboring gene uncharacterized LOC105375128 Neighboring gene uncharacterized LOC100127955 Neighboring gene mitotic arrest deficient 1 like 1 Neighboring gene microRNA 4655

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_120508.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longest transcript.
    Source sequence(s)
    AC074389, BF665480, HY180852, JX046910
  2. NR_120509.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate splice site, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    HO663747, HY180852, JX046910
  3. NR_120510.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) uses an alternate splice site, resulting in a shorter transcript, compared to variant 1.
    Source sequence(s)
    HY180852, JX046910
    Related
    ENST00000453348.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p13 Primary Assembly

    Range
    1738630..1742310 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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