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LOC102723678 uncharacterized LOC102723678 [ Homo sapiens (human) ]

Gene ID: 102723678, updated on 22-Oct-2024

Summary

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Gene symbol
LOC102723678
Gene description
uncharacterized LOC102723678
See related
Ensembl:ENSG00000235659
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
Broad expression in duodenum (RPKM 1.7), small intestine (RPKM 1.7) and 15 other tissues See more
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Genomic context

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See LOC102723678 in Genome Data Viewer
Location:
9q13
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (61865632..61869172, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (41635830..41639300)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379807 Neighboring gene family with sequence similarity 27 member C Neighboring gene family with sequence similarity 27 member E4 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:45003363-45004205 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:45762061-45762809 Neighboring gene uncharacterized LOC107987007 Neighboring gene family with sequence similarity 242 member E

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 studies and variants in dbVar

See Variation Viewer (GRCh38)

Genotypes

NCBI Reference Sequences (RefSeq)

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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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    61865632..61869172 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007061532.1 RNA Sequence

    Related
    ENST00000377547.4

  2. XR_007061533.1 RNA Sequence

  3. XR_950641.3 RNA Sequence

  4. XR_001746498.3 RNA Sequence

    Related
    ENST00000722885.1

  5. XR_001746501.2 RNA Sequence

  6. XR_001746499.2 RNA Sequence

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    41635830..41639300
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_007080378.1 RNA Sequence

  2. XR_007080380.1 RNA Sequence

  3. XR_007080377.1 RNA Sequence

  4. XR_007080379.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

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