QRSL1P1 QRSL1 pseudogene 1 [Homo sapiens (human)] - Gene

Summary

Official Symbol: QRSL1P1provided by HGNC
Official Full Name: QRSL1 pseudogene 1provided by HGNC
Primary source: HGNC:HGNC:43667
See related: Ensembl:ENSG00000215833 AllianceGenome:HGNC:43667
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:: 1q24.2

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	1	NC_000001.11 (168449676..168451315, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	1	NC_060925.1 (167803186..167804825, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	1	NC_000001.10 (168418914..168420553, complement)

Chromosome 1 - NC_000001.11 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

RH104257 (e-PCR)
- UniSTS:98582

RH68838 (e-PCR)
- UniSTS:29778

D1S433 (e-PCR), detects polymorphism
- UniSTS:11613

AL009697 (e-PCR)
- UniSTS:27243

AL009445 (e-PCR)
- UniSTS:9069

SHGC-75876 (e-PCR)
- UniSTS:25984

AFM126yd8 (e-PCR)
- UniSTS:21634

TATC028 (e-PCR)
- UniSTS:498572

SHGC-1539 (e-PCR)
- UniSTS:90005

RH68875 (e-PCR)
- UniSTS:41428

Other Names

glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 pseudogene 1

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.