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    ARAFP2 ARAF pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 644000, updated on 17-Sep-2024

    Summary

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    Official Symbol
    ARAFP2provided by HGNC
    Official Full Name
    ARAF pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:647
    See related
    AllianceGenome:HGNC:647
    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
    PKS1; ARAF2; ARAF2P; ARAFPS
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    Genomic context

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    See ARAFP2 in Genome Data Viewer
    Location:
    7q11.21
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (63404378..63405398, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (64603124..64604144, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (62864756..62865776, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901641 Neighboring gene uncharacterized LOC100287834 Neighboring gene solute carrier family 25 member 1 pseudogene 2 Neighboring gene vomeronasal 1 receptor 33 pseudogene Neighboring gene zinc finger protein 734, pseudogene Neighboring gene septin 7 pseudogene 5

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. The complete sequence and promoter activity of the human A-raf-1 gene (ARAF1). Lee JE, et al. Genomics, 1994 Mar 1. PMID 8020955
    2. Localization of the pKs gene, a raf related sequence on human chromosomes X and 7. Popescu NC, et al. Oncogene, 1989 Apr. PMID 2717185
    3. Sublocalization of an invasion-inducing locus and other genes on human chromosome 7. Habets GG, et al. Cytogenet Cell Genet, 1992. PMID 1505215
    4. Toward a complete human genome sequence. Sanger Center, et al. Genome Res, 1998 Nov. PMID 9847074
    5. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

    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

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    General gene information

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    Markers

    Other Names

    • v-raf murine sarcoma 3611 viral oncogene homolog 2, pseudogene
    • v-raf murine sarcoma 3611 viral oncogene homolog pseudogene

    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_008381.4 

      Range
      101..1121
      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_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      63404378..63405398 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      64603124..64604144 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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