LINC03009 long intergenic non-protein coding RNA 3009 [Homo sapiens (human)] - Gene

Summary

Official Symbol: LINC03009provided by HGNC
Official Full Name: long intergenic non-protein coding RNA 3009provided by HGNC
Primary source: HGNC:HGNC:56134
See related: Ensembl:ENSG00000290873 AllianceGenome:HGNC:56134
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: Ubiquitous expression in testis (RPKM 3.3), fat (RPKM 2.3) and 25 other tissues See more
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Genomic context

Location:: 7q11.23

Exon count:: 3

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	7	NC_000007.14 (76549341..76627982)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	7	NC_060931.1 (77828573..77906904)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	7	NC_000007.13 (76178658..76257299)

Chromosome 7 - NC_000007.14 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Expression

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See details

Project title: Tissue-specific circular RNA induction during human fetal development
Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
BioProject: PRJNA270632
Publication: PMID 26076956
Analysis date: Mon Apr 2 22:54:59 2018

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 variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Markers

ZP3A (e-PCR)
- UniSTS:58634

D7S2875 (e-PCR)
- UniSTS:50957

RH80735 (e-PCR)
- UniSTS:88353

GDB:1318645 (e-PCR)
- UniSTS:63388

STS-U10099 (e-PCR)
- UniSTS:52146

GDB:4585019 (e-PCR)
- UniSTS:17844

D7S2322 (e-PCR)
- UniSTS:82362

RH40786 (e-PCR)
- UniSTS:91867

D7S2308 (e-PCR)
- UniSTS:24312

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.