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CFL1P7 cofilin 1 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 100505919, updated on 13-May-2022

Summary

Official Symbol
CFL1P7provided by HGNC
Official Full Name
cofilin 1 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:39959
See related
AllianceGenome:HGNC:39959
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 CFL1P7 in Genome Data Viewer
Location:
3p24.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (25324119..25325777)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (25326959..25328616)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (25365610..25367268)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene retinoic acid receptor beta Neighboring gene Sharpr-MPRA regulatory region 14202 Neighboring gene Sharpr-MPRA regulatory region 8133 Neighboring gene U7 small nuclear RNA Neighboring gene RNA, 5S ribosomal pseudogene 126

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_028939.1 

    Range
    101..1759
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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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    25324119..25325777
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    25326959..25328616
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)