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MTFR2P1 MTFR2 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100421472, updated on 25-Jan-2022

Summary

Official Symbol
MTFR2P1provided by HGNC
Official Full Name
MTFR2 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:54773
See related
AllianceGenome:HGNC:54773
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See MTFR2P1 in Genome Data Viewer
Location:
2p15
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (63232333..63234030, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (63459468..63461165, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene diazepam binding inhibitor-like 5 pseudogene 2 Neighboring gene WD repeat containing planar cell polarity effector Neighboring gene uncharacterized LOC107985769 Neighboring gene PRELID1 pseudogene 6 Neighboring gene malate dehydrogenase 1

Genomic regions, transcripts, and products

General gene information

Other Names

  • family with sequence similarity 54, member A pseudogene
  • mitochondrial fission regulator 2 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_023562.3 

    Range
    101..1798
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    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_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    63232333..63234030 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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