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OSBPL9P1 oxysterol binding protein like 9 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100130821, updated on 17-Sep-2024

Summary

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Official Symbol
OSBPL9P1provided by HGNC
Official Full Name
oxysterol binding protein like 9 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:48731
See related
Ensembl:ENSG00000271389 AllianceGenome:HGNC:48731
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 OSBPL9P1 in Genome Data Viewer
Location:
3p12.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (80163326..80164975)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (80217927..80219576)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (80212476..80214125)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene roundabout guidance receptor 1 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr3:79667239-79668438 Neighboring gene microRNA 3923 Neighboring gene ReSE screen-validated silencer GRCh37_chr3:79914289-79914466 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:79986556-79987112 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:80101631-80102130 Neighboring gene high mobility group box 1 pseudogene 38 Neighboring gene NANOG hESC enhancer GRCh37_chr3:80312337-80312853 Neighboring gene heterogeneous nuclear ribonucleoprotein A3 pseudogene 8 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:80363655-80364154 Neighboring gene HYDIN pseudogene 1

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)

See Variation Viewer (GRCh38)

General gene information

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Markers

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_022251.3 

    Range
    101..1750
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    80163326..80164975
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    80217927..80219576
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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