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MTCYBP17 MT-CYB pseudogene 17 [ Homo sapiens (human) ]

Gene ID: 107075213, updated on 4-Mar-2025

Summary

Official Symbol
MTCYBP17provided by HGNC
Official Full Name
MT-CYB pseudogene 17provided by HGNC
Primary source
HGNC:HGNC:51970
See related
Ensembl:ENSG00000249247 AllianceGenome:HGNC:51970
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 MTCYBP17 in Genome Data Viewer
Location:
4q32.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (155451617..155452405, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (158784423..158785211, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (156372769..156373557, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene TBC1 domain family member 3C pseudogene Neighboring gene uncharacterized LOC105377503 Neighboring gene MT-ND6 pseudogene 17 Neighboring gene MT-ND5 pseudogene 9

Genomic regions, transcripts, and products

General gene information

Other Names

  • mitochondrially encoded cytochrome b pseudogene 17

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_046499.1 

    Range
    101..889
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    155451617..155452405 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    158784423..158785211 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)