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LOC105373757 uncharacterized LOC105373757 [ Homo sapiens (human) ]

Gene ID: 105373757, updated on 17-Sep-2024

Summary

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Gene symbol
LOC105373757
Gene description
uncharacterized LOC105373757
See related
Ensembl:ENSG00000227098
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Restricted expression toward testis (RPKM 1.6) See more
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Genomic context

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See LOC105373757 in Genome Data Viewer
Location:
2q31.1
Exon count:
10
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (176830842..176849403, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (177312966..177331529, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (177695570..177714131, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene alpha-L-fucosidase 1 pseudogene 1 Neighboring gene ribosomal protein L29 pseudogene 8 Neighboring gene uncharacterized LOC105373756 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:177778427-177778597 Neighboring gene RNA, U6 small nuclear 187, pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues 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

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

Genotypes

General gene information

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Clone Names

  • AC073636.1

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_187986.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636

  2. NR_187987.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636
    Related
    ENST00000659978.1

  3. NR_187988.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636
    Related
    ENST00000661910.1

  4. NR_187989.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636
    Related
    ENST00000665208.1

  5. NR_187990.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636

  6. NR_187991.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636

  7. NR_187992.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636
    Related
    ENST00000661320.1

  8. NR_187993.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636

  9. NR_187994.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636
    Related
    ENST00000661615.1

  10. NR_187995.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636
    Related
    ENST00000457756.2

  11. NR_187996.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636, AC092162
    Related
    ENST00000653543.1

  12. NR_187997.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636, AC092162
    Related
    ENST00000655213.1

  13. NR_187998.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC073636, AC092162

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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    176830842..176849403 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    177312966..177331529 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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