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LOC107986076 rRNA-processing protein FCF1 homolog [ Homo sapiens (human) ]

Gene ID: 107986076, updated on 4-Mar-2025

Summary

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Gene symbol
LOC107986076
Gene description
rRNA-processing protein FCF1 homolog
Gene type
pseudo
RefSeq status
MODEL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See LOC107986076 in Genome Data Viewer
Location:
3p22.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (41401348..41402862, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (41416804..41418318, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:41240699-41241645 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19725 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:41265899-41267098 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:41274918-41276117 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:41290696-41291196 Neighboring gene uncharacterized LOC105377046 Neighboring gene catenin beta 1 Neighboring gene unc-51 like kinase 4 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:41404251-41405010 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr3:41549167-41550366 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:41560057-41560744 Neighboring gene NANOG hESC enhancer GRCh37_chr3:41670520-41671021 Neighboring gene ReSE screen-validated silencer GRCh37_chr3:41737391-41737574 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:41752509-41753118 Neighboring gene RN7SK pseudogene 58 Neighboring gene ATPase H+ transporting V0 subunit e1 pseudogene 2

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

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

NCBI Reference Sequences (RefSeq)

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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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    41401348..41402862 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    41416804..41418318 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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