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FANCD2P2 FANCD2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 101929530, updated on 23-Nov-2021

Summary

Official Symbol
FANCD2P2provided by HGNC
Official Full Name
FANCD2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:44488
See related
Ensembl:ENSG00000230342
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
Low expression observed in reference dataset See more
Orthologs
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Genomic context

See FANCD2P2 in Genome Data Viewer
Location:
3p25.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (11871295..11891197)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (11912769..11932671)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene vestigial like family member 4 Neighboring gene Sharpr-MPRA regulatory region 9131 Neighboring gene TAM41 mitochondrial translocator assembly and maintenance homolog Neighboring gene Sharpr-MPRA regulatory region 5418 Neighboring gene microtubule affinity regulating kinase 2 pseudogene Neighboring gene CYCS pseudogene 12 Neighboring gene nucleoporin 210 pseudogene 2

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

Homology

Other Names

  • Fanconi anemia complementation group D2 pseudogene 2

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_055546.2 

    Range
    101..20003
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    11871295..11891197
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p13 ALT_REF_LOCI_1

Genomic

  1. NW_003871060.2 Reference GRCh38.p13 ALT_REF_LOCI_1

    Range
    95301..115166 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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