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LOC102725532 uncharacterized LOC102725532 [ Homo sapiens (human) ]

Gene ID: 102725532, updated on 23-Nov-2021

Summary

Gene symbol
LOC102725532
Gene description
uncharacterized LOC102725532
See related
Ensembl:ENSG00000236951
Gene type
ncRNA
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

See LOC102725532 in Genome Data Viewer
Location:
Yq11.223
Exon count:
13
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (22101692..22147540, complement)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene elongin C pseudogene 15 Neighboring gene PTPN13 like Y-linked 2 Neighboring gene testis-specific transcript, Y-linked 6B Neighboring gene RNA binding motif protein Y-linked family 1 member F Neighboring gene testis specific protein Y-linked 23, pseudogene

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000024.10 Chromosome Y Reference GRCh38.p13 Primary Assembly

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

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_000024.10 Reference GRCh38.p13 Primary Assembly

    Range
    22101692..22147540 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_001756092.1 RNA Sequence

    Related
    ENST00000419158.1
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