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CPSF6P1 CPSF6 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 133395144, updated on 28-Oct-2024

Summary

Official Symbol
CPSF6P1provided by HGNC
Official Full Name
CPSF6 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:57009
See related
Ensembl:ENSG00000271182 AllianceGenome:HGNC:57009
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 CPSF6P1 in Genome Data Viewer
Location:
19p12
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 19 NC_000019.10 (21634833..21635175, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 19 NC_060943.1 (21773342..21773685, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 19 NC_000019.9 (21817635..21817977, complement)

Chromosome 19 - NC_000019.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904670 Neighboring gene uncharacterized LOC101929007 Neighboring gene uncharacterized LOC105372323 Neighboring gene Sharpr-MPRA regulatory region 12513 Neighboring gene zinc finger protein 100-like Neighboring gene metadherin pseudogene 3

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_242266.1 

    Range
    101..443
    Download
    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_000019.10 Reference GRCh38.p14 Primary Assembly

    Range
    21634833..21635175 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060943.1 Alternate T2T-CHM13v2.0

    Range
    21773342..21773685 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)