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ARAFP2 ARAF pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 644000, updated on 10-Oct-2023

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_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (63404378..63405398, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (64603124..64604144, complement)
105.20220307 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_2023_10

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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