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LOC101930028 uncharacterized LOC101930028 [ Homo sapiens (human) ]

Gene ID: 101930028, updated on 22-Oct-2024

Summary

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Gene symbol
LOC101930028
Gene description
uncharacterized LOC101930028
See related
Ensembl:ENSG00000250626
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 1.1) See more
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Genomic context

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See LOC101930028 in Genome Data Viewer
Location:
4q35.2
Exon count:
8
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (188768982..188818502, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (192122109..192171829, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (189690136..189739656, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene RNA, U7 small nuclear 192 pseudogene Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr4:189655173-189656372 Neighboring gene mitochondrial translation release factor 1 like pseudogene Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_77155 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_77214 Neighboring gene long intergenic non-protein coding RNA 2508 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:189744366-189745364 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:189745365-189746362 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:189862417-189863616 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:189967637-189968466 Neighboring gene uncharacterized LOC105377611 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr4:189979694-189980893 Neighboring gene uncharacterized LOC105377612 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:189981059-189981697

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

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_188358.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC017063, AC093909
    Related
    ENST00000659127.1

  2. NR_188359.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093909
    Related
    ENST00000745576.1

  3. NR_188360.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093909
    Related
    ENST00000745557.1

  4. NR_188361.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093909
    Related
    ENST00000745584.1

  5. NR_188362.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093909

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    188768982..188818502 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    192122109..192171829 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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Molecular Biology Databases
Research Materials