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    CYP4F35P cytochrome P450 family 4 subfamily F member 35, pseudogene [ Homo sapiens (human) ]

    Gene ID: 284233, updated on 17-Jun-2019

    Summary

    Official Symbol
    CYP4F35Pprovided by HGNC
    Official Full Name
    cytochrome P450 family 4 subfamily F member 35, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:39954
    See related
    Ensembl:ENSG00000265787
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Expression
    Broad expression in esophagus (RPKM 2.5), testis (RPKM 1.9) and 19 other tissues See more

    Genomic context

    See CYP4F35P in Genome Data Viewer
    Location:
    18p11.21
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 18 NC_000018.10 (14337423..14342524)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 18 NC_000018.9 (14337422..14342523)

    Chromosome 18 - NC_000018.10Genomic Context describing neighboring genes Neighboring gene ankyrin repeat domain 20 family member A5, pseudogene Neighboring gene ras homolog family member T1 pseudogene 1 Neighboring gene sorting nexin 18 pseudogene Neighboring gene zinc finger protein 114 pseudogene Neighboring gene family with sequence similarity 207 member A pseudogene

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    General gene information

    Markers

    Other Names

    • CYP4F-se8[6:7:8]
    • cytochrome P450, family 4, subfamily F, polypeptide 35, pseudogene

    NCBI Reference Sequences (RefSeq)

    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.

    RNA

    1. NR_026756.1 RNA Sequence

      Status: INFERRED

      Source sequence(s)
      AP005212
      Related
      ENST00000582957.1

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000018.10 Reference GRCh38.p13 Primary Assembly

      Range
      14337423..14342524
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_030000.1: Suppressed sequence

      Description
      NG_030000.1: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.
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