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MCF2L-AS1 MCF2L antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 100289410, updated on 9-Jan-2022

Summary

Official Symbol
MCF2L-AS1provided by HGNC
Official Full Name
MCF2L antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:39825
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See MCF2L-AS1 in Genome Data Viewer
Location:
13q34
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 13 NC_000013.11 (112967484..112968638, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (113621798..113622952, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene ATPase phospholipid transporting 11A Neighboring gene Sharpr-MPRA regulatory region 8271 Neighboring gene ATP11A antisense RNA 1 Neighboring gene MCF.2 cell line derived transforming sequence like Neighboring gene uncharacterized LOC107984591 Neighboring gene proline-rich extensin-like protein EPR1

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

General gene information

Markers

Other Names

  • MCF2L antisense RNA 1 (non-protein coding)

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_034002.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL356740, BC004179, BQ012856

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_000013.11 Reference GRCh38.p13 Primary Assembly

    Range
    112967484..112968638 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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