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RPL7L1P11 ribosomal protein L7 like 1 pseudogene 11 [ Homo sapiens (human) ]

Gene ID: 347509, updated on 13-May-2022

Summary

Official Symbol
RPL7L1P11provided by HGNC
Official Full Name
ribosomal protein L7 like 1 pseudogene 11provided by HGNC
Primary source
HGNC:HGNC:39493
See related
AllianceGenome:HGNC:39493
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

See RPL7L1P11 in Genome Data Viewer
Location:
Xq28
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (148464669..148465581)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (146729270..146730182)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (147546189..147547101)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ferritin heavy chain 1 pseudogene 8 Neighboring gene HAX1 pseudogene 1 Neighboring gene origin of replication in 5' region of AFF2/FMR2 Neighboring gene fragile site, folic acid type, rare, fra(X)(q28) E Neighboring gene AF4/FMR2 family member 2 Neighboring gene RN7SK pseudogene 267

Genomic regions, transcripts, and products

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_009927.3 

    Range
    101..1013
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    148464669..148465581
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    146729270..146730182
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)