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LOC101928475 uncharacterized LOC101928475 [ Homo sapiens (human) ]

Gene ID: 101928475, updated on 22-Oct-2024

Summary

Gene symbol
LOC101928475
Gene description
uncharacterized LOC101928475
See related
Ensembl:ENSG00000232058
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Annotation information
Annotation category: partial on reference assembly
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Genomic context

See LOC101928475 in Genome Data Viewer
Location:
17p12
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (15051355..15052276)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (14957375..14958296)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (14954672..14955593)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene ribosomal protein L23a pseudogene 76 Neighboring gene CMT1A duplicated region transcript 7 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr17:15009287-15010486 Neighboring gene CMT1A duplicated region transcript 8 Neighboring gene uncharacterized LOC107984976

Genomic regions, transcripts, and products

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_135638.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    BC033345, BG722758
    Related
    ENST00000446671.2

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    15051355..15052276
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    14957375..14958296
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)