Format

Send to:

Choose Destination

FUNDC2P2 FUN14 domain containing 2 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 388965, updated on 24-Jul-2021

Summary

Official Symbol
FUNDC2P2provided by HGNC
Official Full Name
FUN14 domain containing 2 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:17247
Gene type
pseudo
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See FUNDC2P2 in Genome Data Viewer
Location:
2p11.2
Exon count:
1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (84290682..84292200)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (84517806..84519324)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 pseudogene 1 Neighboring gene CRLF3 pseudogene 3 Neighboring gene uncharacterized LOC107985905 Neighboring gene succinate-CoA ligase GDP/ADP-forming subunit alpha Neighboring gene dynein axonemal heavy chain 6 Neighboring gene uncharacterized LOC107985906

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_003663.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC097458

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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
    84290682..84292200
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001013648.3: Suppressed sequence

    Description
    NM_001013648.3: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
Support Center