OSBPL9P2 oxysterol binding protein like 9 pseudogene 2 [Homo sapiens (human)] - Gene

Summary

Official Symbol: OSBPL9P2provided by HGNC
Official Full Name: oxysterol binding protein like 9 pseudogene 2provided by HGNC
Primary source: HGNC:HGNC:48732
See related: AllianceGenome:HGNC:48732
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

Location:: 11q14.3

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	11	NC_000011.10 (91113876..91116002, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	11	NC_060935.1 (91035430..91037589, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	11	NC_000011.9 (90847044..90849170, complement)

Chromosome 11 - NC_000011.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

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

D11S4952 (e-PCR)
- UniSTS:46360

G63474 (e-PCR)
- UniSTS:140586

SHGC-148962 (e-PCR)
- UniSTS:176707

RH44964 (e-PCR)
- UniSTS:89982

D11S1259 (e-PCR)
- UniSTS:148352

D11S1825 (e-PCR)
- UniSTS:148868

RH122463 (e-PCR)
- UniSTS:135335

D11S4037 (e-PCR)
- UniSTS:68339

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.