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MYL12-AS1 MYL12A and MYL12B antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 104968399, updated on 23-Nov-2021

Summary

Official Symbol
MYL12-AS1provided by HGNC
Official Full Name
MYL12A and MYL12B antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:55331
See related
Ensembl:ENSG00000264235
Gene type
ncRNA
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 heart (RPKM 149.6), lung (RPKM 55.7) and 23 other tissues See more
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Genomic context

See MYL12-AS1 in Genome Data Viewer
Location:
18p11.31
Exon count:
5
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 18 NC_000018.10 (3255436..3262359, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (3255434..3262357, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene myomesin 1 Neighboring gene RNA, U7 small nuclear 25 pseudogene Neighboring gene uncharacterized LOC101927044 Neighboring gene myosin light chain 12A Neighboring gene myosin light chain 12B Neighboring gene Sharpr-MPRA regulatory region 9674 Neighboring gene CRISPRi-validated cis-regulatory element chr18.117

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_130143.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longest transcript.
    Source sequence(s)
    AP005329
    Related
    ENST00000578800.6
  2. NR_130144.2 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate splice site in the first exon compared to variant 2.
    Source sequence(s)
    AP005329
    Related
    ENST00000581905.2
  3. NR_130145.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) uses an alternate 5' most exon and lacks an internal segment in the 5' region, compared to variant 1.
    Source sequence(s)
    AL550084, BG218162, BI908211, HY010228, HY167137

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_000018.10 Reference GRCh38.p13 Primary Assembly

    Range
    3255436..3262359 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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