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FAR2P2 fatty acyl-CoA reductase 2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100216479, updated on 23-Nov-2021

Summary

Official Symbol
FAR2P2provided by HGNC
Official Full Name
fatty acyl-CoA reductase 2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:49279
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Broad expression in testis (RPKM 8.4), prostate (RPKM 7.7) and 15 other tissues See more
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Genomic context

See FAR2P2 in Genome Data Viewer
Location:
2q21.1
Exon count:
6
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (130416750..130428546, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (131174323..131186119, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene protein tyrosine phosphatase non-receptor type 18 Neighboring gene uncharacterized LOC105373618 Neighboring gene Kruppel like factor 2 pseudogene 2 Neighboring gene cytochrome P450 family 4 subfamily F member 62, pseudogene Neighboring gene POTE ankyrin domain family member I Neighboring gene RNA, U6 small nuclear 473, 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

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.

RNA

  1. NR_046258.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longest transcript.
    Source sequence(s)
    AC132479, AL704735, BM678458, CN315133, DA416892, DA522902
  2. NR_046259.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) lacks an internal exon in the 5' region, compared to variant 1.
    Source sequence(s)
    AC132479, AL704735, BM678458, CN315133, DA416892, DA866260
  3. NR_046260.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (3) lacks two consecutive internal exons in the 5' region, compared to variant 1.
    Source sequence(s)
    AK054990, AL704735, BM678458, DA065395, DA416892

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    130416750..130428546 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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