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RN7SL825P RNA, 7SL, cytoplasmic 825, pseudogene [ Homo sapiens (human) ]

Gene ID: 107080654, updated on 10-Dec-2024

Summary

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Official Symbol
RN7SL825Pprovided by HGNC
Official Full Name
RNA, 7SL, cytoplasmic 825, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:46841
See related
Ensembl:ENSG00000239731 AllianceGenome:HGNC:46841
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See RN7SL825P in Genome Data Viewer
Location:
10p11.22
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (31992087..31992381, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (32020744..32021038, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (32281015..32281309, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene Rho GTPase activating protein 12 Neighboring gene uncharacterized LOC107984219 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2280 Neighboring gene high mobility group box 1 pseudogene 7 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr10:32229391-32230590 Neighboring gene uncharacterized LOC105376485 Neighboring gene ribosomal protein L34 pseudogene 19 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:32291606-32292421 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:32306942-32308141 Neighboring gene kinesin family member 5B Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr10:32337050-32338249 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3244 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2281 Neighboring gene ribosomal protein S4X pseudogene 11

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

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 (GRCh37.p13)

General gene information

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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.

Genomic

  1. NG_046567.1 

    Range
    101..395
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    31992087..31992381 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    32020744..32021038 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Other Literature Sources
Molecular Biology Databases