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HOTS H19 opposite tumor suppressor [ Homo sapiens (human) ]

Gene ID: 103344718, discontinued on 20-Jun-2020
  • This record has been withdrawn by NCBI. It was defined by NM_001293171.2, for which there is insufficient evidence to establish a distinct locus separate from the broader transcription seen in this region.

Summary

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Gene symbol
HOTS
Gene description
H19 opposite tumor suppressor
Gene type
protein coding
RefSeq status
WITHDRAWN
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
DISCONTINUED: This record has been withdrawn by NCBI. It was defined by NM_001293171.2, for which there is insufficient evidence to establish a distinct locus separate from the broader transcription seen in this region.
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Genomic context

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Location:
11p15.5
Exon count:
1
Annotation release Status Assembly Chr Location
109.20200522 latest, but not current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (1992408..1996294)

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. HOTS (H19 Opposite Tumor Suppressor) encodes a tumor growth inhibitor that localizes to the nucleus and nucleolus and that interacts with the human enhancer of rudimentary homolog (ERH) protein.
    Title: A nucleolar protein, H19 opposite tumor suppressor (HOTS), is a tumor growth inhibitor encoded by a human imprinted H19 antisense transcript.
Submit: New GeneRIF Correction

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See Variation Viewer (GRCh38)

Genotypes

General protein information

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Names
H19 opposite tumor suppressor

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20200522 (NOTE: not current)

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    1992408..1996294
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001293171.2 → NP_001280100.1  

Reference GRCh38.p13 PATCHES

Genomic

  1. NW_021160004.1 Reference GRCh38.p13 PATCHES

    Range
    184930..188816
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001293171.2 → NP_001280100.1  

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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