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LOC399900 uncharacterized LOC399900 [ Homo sapiens (human) ]

Gene ID: 399900, updated on 23-Nov-2021

Summary

Gene symbol
LOC399900
Gene description
uncharacterized LOC399900
See related
Ensembl:ENSG00000279491
Gene type
ncRNA
RefSeq status
MODEL
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 LOC399900 in Genome Data Viewer
Location:
11q12.3
Exon count:
1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (61967798..61969370)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene bestrophin 1 Neighboring gene uncharacterized LOC107984334 Neighboring gene ferritin heavy chain 1 Neighboring gene NFE2L2 motif-containing MPRA enhancer 20 Neighboring gene ribosomal protein S2 pseudogene 37

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000011.10 Chromosome 11 Reference GRCh38.p13 Primary Assembly

NCBI Reference Sequences (RefSeq)

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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_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    61967798..61969370
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_247232.4 RNA Sequence

    Related
    ENST00000623785.1

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001013667.1: Suppressed sequence

    Description
    NM_001013667.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
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