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MTCYBP29 MT-CYB pseudogene 29 [ Homo sapiens (human) ]

Gene ID: 107075135, updated on 10-Oct-2023

Summary

Official Symbol
MTCYBP29provided by HGNC
Official Full Name
MT-CYB pseudogene 29provided by HGNC
Primary source
HGNC:HGNC:51995
See related
Ensembl:ENSG00000224880 AllianceGenome:HGNC:51995
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 MTCYBP29 in Genome Data Viewer
Location:
7p11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (57173357..57174362)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (57416635..57417640)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (57241064..57242069)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene GUSB pseudogene 10 Neighboring gene MT-ND5 pseudogene 6 Neighboring gene MT-ND6 pseudogene 29 Neighboring gene nuclear-encoded mitochondrial tRNA-Gln (TTG) 13-1 Neighboring gene MT-ND1 pseudogene 4

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded cytochrome b pseudogene 29

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_046507.1 

    Range
    101..1106
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    57173357..57174362
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    57416635..57417640
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)