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TOMM22P5 TOMM22 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 390007, updated on 13-May-2022

Summary

Official Symbol
TOMM22P5provided by HGNC
Official Full Name
TOMM22 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:38741
See related
AllianceGenome:HGNC:38741
Gene type
pseudo
RefSeq status
INFERRED
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 TOMM22P5 in Genome Data Viewer
Location:
10q26.11
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (118643759..118644394)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (119538891..119539526)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (120403271..120403906)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene solute carrier family 25 member 18 pseudogene 1 Neighboring gene prolactin releasing hormone receptor Neighboring gene CDK2 associated cullin domain 1 Neighboring gene Sharpr-MPRA regulatory region 11808

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • translocase of outer mitochondrial membrane 22 homolog pseudogene 5

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_023452.2 

    Range
    101..736
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    118643759..118644394
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    119538891..119539526
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)