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    FECHP1 ferrochelatase pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 2236, updated on 10-Oct-2023

    Summary

    Official Symbol
    FECHP1provided by HGNC
    Official Full Name
    ferrochelatase pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:3648
    See related
    AllianceGenome:HGNC:3648
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    FECHP
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    Genomic context

    Location:
    3p22.3
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (34872581..34875228)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (34873545..34876192)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (34914073..34916720)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC102724048 Neighboring gene ReSE screen-validated silencer GRCh37_chr3:34661590-34661813 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:34682175-34682809 Neighboring gene uncharacterized LOC124909365 Neighboring gene uncharacterized LOC101928135 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:35187219-35187720 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:35187721-35188220 Neighboring gene keratin 8 pseudogene 18 Neighboring gene RNA, U6 small nuclear 243, pseudogene

    Genomic regions, transcripts, and products

    Phenotypes

    EBI GWAS Catalog

    Description
    Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD.
    EBI GWAS Catalog
    Heritability and genetic association analysis of cognition in the Diabetes Heart Study.
    EBI GWAS Catalog

    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_001118.7 

      Range
      101..2748
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

    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
      34872581..34875228
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060927.1 Alternate T2T-CHM13v2.0

      Range
      34873545..34876192
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)