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MILIP MYC inducible lncRNA inactivating p53 [ Homo sapiens (human) ]

Gene ID: 92659, updated on 29-Jan-2023

Summary

Official Symbol
MILIPprovided by HGNC
Official Full Name
MYC inducible lncRNA inactivating p53provided by HGNC
Primary source
HGNC:HGNC:43649
See related
Ensembl:ENSG00000265688 AllianceGenome:HGNC:43649
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
MAFG-DT; MAFG-AS1
Expression
Broad expression in testis (RPKM 2.2), thyroid (RPKM 0.6) and 19 other tissues See more
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Genomic context

See MILIP in Genome Data Viewer
Location:
17q25.3
Exon count:
2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (81927829..81930753)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (82794988..82797912)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (79885705..79888629)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene phosphate cytidylyltransferase 2, ethanolamine Neighboring gene neuropeptide B Neighboring gene sirtuin 7 Neighboring gene MAF bZIP transcription factor G Neighboring gene pyrroline-5-carboxylate reductase 1 Neighboring gene myeloid associated differentiation marker like 2

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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

General gene information

Markers

Other Names

  • MAFG antisense RNA 1 (head to head)
  • MAFG antisense RNA 1 (non-protein coding)
  • MAFG divergent transcript
  • c-Myc-Inducible Long noncoding RNA Inactivating P53

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_015454.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC009233, BC046361, BC134411
    Related
    ENST00000582106.1

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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    81927829..81930753
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    82794988..82797912
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)