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LOC729774 SLX9 ribosome biogenesis factor pseudogene [ Homo sapiens (human) ]

Gene ID: 729774, updated on 17-Sep-2024

Summary

Gene symbol
LOC729774
Gene description
SLX9 ribosome biogenesis factor pseudogene
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 LOC729774 in Genome Data Viewer
Location:
18p11.21
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 18 NC_000018.10 (14361247..14361945, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 18 NC_060942.1 (14524111..14524809, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (14361246..14361944, complement)

Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene cytochrome P450 family 4 subfamily F member 35, pseudogene Neighboring gene zinc finger protein 114 pseudogene Neighboring gene TERF1 pseudogene 2 Neighboring gene fem-1 homolog A pseudogene 2

Genomic regions, transcripts, and products

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_022480.3 

    Range
    101..799
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    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_000018.10 Reference GRCh38.p14 Primary Assembly

    Range
    14361247..14361945 complement
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060942.1 Alternate T2T-CHM13v2.0

    Range
    14524111..14524809 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)