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CYTB cytochrome b [ Homo sapiens neanderthalensis (Neandertal) ]

Gene ID: 6775065, updated on 3-Apr-2024

Summary

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Gene symbol
CYTB
Gene description
cytochrome b
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens neanderthalensis (common: Neandertal, sub-species: neanderthalensis)
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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Sequence:
Chromosome: MT; NC_011137.1 (14742..15882)

Chromosome MT - NC_011137.1Genomic Context describing neighboring genes Neighboring gene NADH dehydrogenase subunit 6 Neighboring gene tRNA-Glu Neighboring gene tRNA-Thr Neighboring gene tRNA-Pro

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_011137.1

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder. Rollins B, et al. PLoS One, 2009. PMID 19290059, Free PMC Article
  2. Do mitochondrial mutations cause recurrent miscarriage? Kaare M, et al. Mol Hum Reprod, 2009 May. PMID 19297417
  3. Genotyping mitochondrial DNA single nucleotide polymorphisms by PCR ligase detection reactions. Luo Y, et al. Clin Chem Lab Med, 2010 Apr. PMID 20128730
  4. Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss. Kato T, et al. J Hum Genet, 2010 Mar. PMID 20111055
  5. A complete Neandertal mitochondrial genome sequence determined by high-throughput sequencing. Green RE, et al. Cell, 2008 Aug 8. PMID 18692465, Free PMC Article

See all (7) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Observational study of gene-disease association and genetic testing. (HuGE Navigator)
    Title: Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
  2. Observational study of genetic testing. (HuGE Navigator)
    Title: Genotyping mitochondrial DNA single nucleotide polymorphisms by PCR ligase detection reactions.
  3. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
    Title: Involvement of mitochondrial DNA sequence variations and respiratory activity in late complications following radiotherapy.
  4. Observational study of gene-disease association. (HuGE Navigator)
    Title: Do mitochondrial mutations cause recurrent miscarriage?
Submit: New GeneRIF Correction

General protein information

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Preferred Names
cytochrome b
YP_002124314.2
  • TAA stop codon is completed by the addition of 3' A residues to the mRNA

NCBI Reference Sequences (RefSeq)

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Genome Annotation

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

Reference assembly

Genomic

  1. NC_011137.1 Reference assembly

    Range
    14742..15882
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. YP_002124314.2 cytochrome b (mitochondrion) [Homo sapiens neanderthalensis]

    See identical proteins and their annotated locations for YP_002124314.2

    Status: REVIEWED

    UniProtKB/TrEMBL
    A0A059UG11, A0A343EQI1, A0A7G5XR64
    Conserved Domains (1) summary
    MTH00100
    Location:1 → 379
    CYTB; cytochrome b; Provisional
Nucleotide Protein
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Gene LinkOut

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Research Materials