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LOC389199 uncharacterized LOC389199 [ Homo sapiens (human) ]

Gene ID: 389199, updated on 13-May-2022

Summary

Gene symbol
LOC389199
Gene description
uncharacterized LOC389199
See related
Ensembl:ENSG00000228919
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Orthologs
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Genomic context

See LOC389199 in Genome Data Viewer
Location:
4p16.1
Exon count:
1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (7939001..7940296)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (7917546..7918841)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (7940728..7942023)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene actin filament associated protein 1 Neighboring gene uncharacterized LOC124900656 Neighboring gene Sharpr-MPRA regulatory region 8435 Neighboring gene Sharpr-MPRA regulatory region 14367 Neighboring gene Sharpr-MPRA regulatory region 6491 Neighboring gene uncharacterized LOC124900657 Neighboring gene actin binding LIM protein family member 2

Genomic regions, transcripts, and products

General gene information

Homology

Clone Names

  • MGC35057, AC097381.1

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_172651.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC097381
    Related
    ENST00000429019.4

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    7939001..7940296
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    7917546..7918841
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_203423.2: Suppressed sequence

    Description
    NM_203423.2: This RefSeq was removed because it is now thought that this gene does not encode a protein.