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GOT2P7 GOT2 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 100422628, updated on 23-Nov-2021

Summary

Official Symbol
GOT2P7provided by HGNC
Official Full Name
GOT2 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:54892
See related
Ensembl:ENSG00000232392
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 GOT2P7 in Genome Data Viewer
Location:
Xp22.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (11334036..11335999, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (11352156..11354119, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene Rho GTPase activating protein 6 Neighboring gene amelogenin X-linked Neighboring gene microRNA 548ax Neighboring gene Sharpr-MPRA regulatory region 12383 Neighboring gene NFE2L2 motif-containing MPRA enhancer 58

Genomic regions, transcripts, and products

General gene information

Other Names

  • glutamic-oxaloacetic transaminase 2, mitochondrial (aspartate aminotransferase 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_026658.2 

    Range
    101..2064
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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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    11334036..11335999 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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