Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, an... See more...

Aliases for COX6B1 Gene

Aliases for COX6B1 Gene

  • Cytochrome C Oxidase Subunit 6B1 2 3 4 5
  • Cytochrome C Oxidase Subunit VIb Polypeptide 1 (Ubiquitous) 2 3
  • COX VIb-1 3 4
  • COX6B 3 4
  • COXG 2 3
  • Cytochrome C Oxidase Subunit Vib Polypeptide 1 (Ubiquitous) 2
  • Cytochrome C Oxidase Subunit VIb Isoform 1 4
  • Cytochrome C Oxidase Subunit Vib 2
  • COXVIb1 3
  • COX6B1 5

External Ids for COX6B1 Gene

Previous HGNC Symbols for COX6B1 Gene

  • COX6B

Previous GeneCards Identifiers for COX6B1 Gene

  • GC19P040831
  • GC19P036140
  • GC19P032644
  • GC19P035696
  • GC19P035821
  • GC19P037017
  • GC19P037186
  • GC19P037282
  • GC19P037718
  • GC19P035844
  • GC19P035999
  • GC19P036166
  • GC19P036238
  • GC19P036408
  • GC19P036569
  • GC19P036737
  • GC19P036883

Summaries for COX6B1 Gene

Entrez Gene Summary for COX6B1 Gene

  • Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. This nuclear gene encodes subunit VIb. Mutations in this gene are associated with severe infantile encephalomyopathy. Three pseudogenes COX6BP-1, COX6BP-2 and COX6BP-3 have been found on chromosomes 7, 17 and 22q13.1-13.2, respectively. [provided by RefSeq, Jan 2010]

GeneCards Summary for COX6B1 Gene

COX6B1 (Cytochrome C Oxidase Subunit 6B1) is a Protein Coding gene. Diseases associated with COX6B1 include Mitochondrial Complex Iv Deficiency and Leigh Syndrome. Among its related pathways are Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. and Cardiac muscle contraction. Gene Ontology (GO) annotations related to this gene include cytochrome-c oxidase activity. An important paralog of this gene is COX6B2.

UniProtKB/Swiss-Prot Summary for COX6B1 Gene

  • Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and the ATP synthase. Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Electrons originating from reduced cytochrome c in the intermembrane space (IMS) are transferred via the dinuclear copper A center (CU(A)) of subunit 2 and heme A of subunit 1 to the active site in subunit 1, a binuclear center (BNC) formed by heme A3 and copper B (CU(B)). The BNC reduces molecular oxygen to 2 water molecules using 4 electrons from cytochrome c in the IMS and 4 protons from the mitochondrial matrix.

Gene Wiki entry for COX6B1 Gene

No data available for CIViC Summary , Tocris Summary , PharmGKB "VIP" Summary , Rfam classification and piRNA Summary for COX6B1 Gene

Genomics for COX6B1 Gene

GeneHancer (GH) Regulatory Elements Pubs

Promoters and enhancers for COX6B1 Gene
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around COX6B1 on the GeneHancer Hub at the UCSC Golden Path

Cistromic (ChIP-Seq) regulation report from SPP (The Signaling Pathways Project) for COX6B1

Top Transcription factor binding sites by QIAGEN in the COX6B1 gene promoter:
  • c-Ets-1
  • E2F
  • E2F-1
  • E2F-2
  • E2F-3a
  • E2F-4
  • E2F-5
  • GATA-2
  • HTF
  • RelA

Genomic Locations for COX6B1 Gene

Genomic Locations for COX6B1 Gene
chr19:35,648,323-35,658,782
(GRCh38/hg38)
Size:
10,460 bases
Orientation:
Plus strand
chr19:36,139,125-36,149,763
(GRCh37/hg19)
Size:
10,639 bases
Orientation:
Plus strand

Genomic View for COX6B1 Gene

Genes around COX6B1 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
COX6B1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for COX6B1 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for COX6B1 Gene

Proteins for COX6B1 Gene

  • Protein details for COX6B1 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    P14854-CX6B1_HUMAN
    Recommended name:
    Cytochrome c oxidase subunit 6B1
    Protein Accession:
    P14854
    Secondary Accessions:
    • B2R5C9
    • Q6IBL4

    Protein attributes for COX6B1 Gene

    Size:
    86 amino acids
    Molecular mass:
    10192 Da
    Quaternary structure:
    • Component of the cytochrome c oxidase (complex IV, CIV), a multisubunit enzyme composed of 14 subunits. The complex is composed of a catalytic core of 3 subunits MT-CO1, MT-CO2 and MT-CO3, encoded in the mitochondrial DNA, and 11 supernumerary subunits COX4I1 (or COX4I2), COX5A, COX5B, COX6A1 (or COX6A2), COX6B1 (or COX6B2), COX6C, COX7A2 (or COX7A1), COX7B, COX7C, COX8A and NDUFA4, which are encoded in the nuclear genome (PubMed:30030519). The complex exists as a monomer or a dimer and forms supercomplexes (SCs) in the inner mitochondrial membrane with NADH-ubiquinone oxidoreductase (complex I, CI) and ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII), resulting in different assemblies (supercomplex SCI(1)III(2)IV(1) and megacomplex MCI(2)III(2)IV(2)) (PubMed:28844695).

    Three dimensional structures from OCA and Proteopedia for COX6B1 Gene

neXtProt entry for COX6B1 Gene

Post-translational modifications for COX6B1 Gene

  • Ubiquitination at Lys8 and Lys47
  • Modification sites at PhosphoSitePlus

Other Protein References for COX6B1 Gene

No data available for DME Specific Peptides for COX6B1 Gene

Domains & Families for COX6B1 Gene

Gene Families for COX6B1 Gene

HGNC:
Human Protein Atlas (HPA):
  • Disease related genes
  • Plasma proteins
  • Predicted intracellular proteins

Protein Domains for COX6B1 Gene

InterPro:
Blocks:
  • Cytochrome oxidase c, subunit VIb
ProtoNet:

Suggested Antigen Peptide Sequences for COX6B1 Gene

GenScript: Design optimal peptide antigens:
  • Cytochrome c oxidase subunit VIb isoform 1 (CX6B1_HUMAN)

Graphical View of Domain Structure for InterPro Entry

P14854

UniProtKB/Swiss-Prot:

CX6B1_HUMAN :
  • Belongs to the cytochrome c oxidase subunit 6B family.
Family:
  • Belongs to the cytochrome c oxidase subunit 6B family.
genes like me logo Genes that share domains with COX6B1: view

Function for COX6B1 Gene

Molecular function for COX6B1 Gene

UniProtKB/Swiss-Prot Function:
Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and the ATP synthase. Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Electrons originating from reduced cytochrome c in the intermembrane space (IMS) are transferred via the dinuclear copper A center (CU(A)) of subunit 2 and heme A of subunit 1 to the active site in subunit 1, a binuclear center (BNC) formed by heme A3 and copper B (CU(B)). The BNC reduces molecular oxygen to 2 water molecules using 4 electrons from cytochrome c in the IMS and 4 protons from the mitochondrial matrix.

Phenotypes From GWAS Catalog for COX6B1 Gene

Gene Ontology (GO) - Molecular Function for COX6B1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0004129 cytochrome-c oxidase activity NAS 2172092
genes like me logo Genes that share ontologies with COX6B1: view
genes like me logo Genes that share phenotypes with COX6B1: view

Human Phenotype Ontology for COX6B1 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Model Products

CRISPR Products

miRNA for COX6B1 Gene

miRTarBase miRNAs that target COX6B1

Inhibitory RNA Products

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for COX6B1

No data available for Enzyme Numbers (IUBMB) , Animal Models , Transcription Factor Targets and HOMER Transcription for COX6B1 Gene

Localization for COX6B1 Gene

Subcellular locations from UniProtKB/Swiss-Prot for COX6B1 Gene

Mitochondrion inner membrane. Peripheral membrane protein. Intermembrane side.

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for COX6B1 gene
Compartment Confidence
mitochondrion 5
extracellular 3
nucleus 2
cytosol 2
plasma membrane 1
cytoskeleton 1
peroxisome 1
endoplasmic reticulum 1
golgi apparatus 1

Subcellular locations from the

Human Protein Atlas (HPA)

Gene Ontology (GO) - Cellular Components for COX6B1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005739 mitochondrion IEA,IBA 21873635
GO:0005743 mitochondrial inner membrane TAS --
GO:0016020 membrane IEA --
GO:0045277 respiratory chain complex IV IBA 21873635
genes like me logo Genes that share ontologies with COX6B1: view

Pathways & Interactions for COX6B1 Gene

genes like me logo Genes that share pathways with COX6B1: view

UniProtKB/Swiss-Prot P14854-CX6B1_HUMAN

  • Pathway: Energy metabolism; oxidative phosphorylation.

Interacting Proteins for COX6B1 Gene

Gene Ontology (GO) - Biological Process for COX6B1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0006119 oxidative phosphorylation IEA --
GO:0006123 mitochondrial electron transport, cytochrome c to oxygen TAS --
GO:0021762 substantia nigra development HEP 22926577
GO:1902600 proton transmembrane transport IEA --
genes like me logo Genes that share ontologies with COX6B1: view

No data available for SIGNOR curated interactions for COX6B1 Gene

Drugs & Compounds for COX6B1 Gene

(4) Drugs for COX6B1 Gene - From: DrugBank and HMDB

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
cholic acid Approved Pharma Agonist, Full agonist, Target 0
Oxygen Approved, Vet_approved Pharma 0
Water Approved Pharma 0
N-Formylmethionine Experimental Pharma Target 0
genes like me logo Genes that share compounds with COX6B1: view

Transcripts for COX6B1 Gene

mRNA/cDNA for COX6B1 Gene

1 REFSEQ mRNAs :
10 NCBI additional mRNA sequence :
5 Ensembl transcripts including schematic representations, and UCSC links to gene/alias where relevant :

CRISPR Products

Inhibitory RNA Products

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for COX6B1

Alternative Splicing Database (ASD) splice patterns (SP) for COX6B1 Gene

ExUns: 1a · 1b ^ 2 ^ 3 ^ 4
SP1:
SP2: -

Relevant External Links for COX6B1 Gene

GeneLoc Exon Structure for
COX6B1

Expression for COX6B1 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and SAGE for COX6B1 Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

Protein differential expression in normal tissues from HIPED for COX6B1 Gene

This gene is overexpressed in Peripheral blood mononuclear cells (11.3) and Liver, secretome (9.5).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, MaxQB, and MOPED for COX6B1 Gene



Protein tissue co-expression partners for COX6B1 Gene

- Elite partner

Transcriptomic regulation report from SPP (The Signaling Pathways Project) for COX6B1

SOURCE GeneReport for Unigene cluster for COX6B1 Gene:

Hs.431668

Evidence on tissue expression from TISSUES for COX6B1 Gene

  • Nervous system(4.9)
  • Muscle(4.8)
  • Liver(4.6)
  • Kidney(4.6)
  • Blood(4.5)
  • Eye(4.4)
  • Heart(3.6)
  • Skin(3.1)
  • Intestine(2.4)
  • Stomach(2.4)
  • Lymph node(2.3)
  • Spleen(2.3)
  • Bone marrow(2)

Phenotype-based relationships between genes and organs from Gene ORGANizer for COX6B1 Gene

Germ Layers:
  • ectoderm
  • endoderm
  • mesoderm
Systems:
  • cardiovascular
  • digestive
  • immune
  • integumentary
  • nervous
  • respiratory
  • skeletal muscle
  • urinary
Regions:
Head and neck:
  • brain
  • cerebrospinal fluid
  • cranial nerve
  • ear
  • eye
  • eyelid
  • face
  • head
  • meninges
  • neck
Thorax:
  • bronchus
  • heart
  • heart valve
  • lung
  • trachea
Abdomen:
  • kidney
  • liver
General:
  • blood
  • blood vessel
  • coagulation system
  • peripheral nervous system
  • red blood cell
  • skin
genes like me logo Genes that share expression patterns with COX6B1: view

No data available for mRNA differential expression in normal tissues and mRNA Expression by UniProt/SwissProt for COX6B1 Gene

Orthologs for COX6B1 Gene

This gene was present in the common ancestor of eukaryotes.

Orthologs for COX6B1 Gene

Organism Taxonomy Gene Similarity Type Details
Chimpanzee
(Pan troglodytes)
Mammalia COX6B1 30 31
  • 99.61 (n)
OneToOne
Dog
(Canis familiaris)
Mammalia LOC612644 30
  • 89.53 (n)
-- 31
  • 85 (a)
OneToMany
-- 31
  • 76 (a)
OneToMany
Cow
(Bos Taurus)
Mammalia COX6B1 30 31
  • 89.15 (n)
OneToMany
-- 31
  • 83 (a)
OneToMany
Mouse
(Mus musculus)
Mammalia Cox6b1 30 17 31
  • 85.66 (n)
OneToOne
Rat
(Rattus norvegicus)
Mammalia LOC688869 30
  • 85.66 (n)
Oppossum
(Monodelphis domestica)
Mammalia COX6B1 31
  • 77 (a)
OneToOne
Platypus
(Ornithorhynchus anatinus)
Mammalia COX6B1 31
  • 72 (a)
OneToOne
Lizard
(Anolis carolinensis)
Reptilia COX6B1 31
  • 67 (a)
OneToOne
Tropical Clawed Frog
(Silurana tropicalis)
Amphibia cox6b1 30
  • 66.28 (n)
Str.6264 30
African clawed frog
(Xenopus laevis)
Amphibia Xl.34724 30
Zebrafish
(Danio rerio)
Actinopterygii cox6b1 30 31
  • 69.38 (n)
OneToOne
wufa92g05 30
African malaria mosquito
(Anopheles gambiae)
Insecta AgaP_AGAP013092 30
  • 67.14 (n)
Fruit Fly
(Drosophila melanogaster)
Insecta CoVIb 30 31
  • 64.79 (n)
OneToMany
Worm
(Caenorhabditis elegans)
Secernentea Y71H2AM.5 31
  • 26 (a)
OneToMany
K. Lactis Yeast
(Kluyveromyces lactis)
Saccharomycetes KLLA0F17281g 30
  • 57.5 (n)
A. gosspyii yeast
(Eremothecium gossypii)
Saccharomycetes AGOS_ADR240C 30
  • 57.49 (n)
Baker's yeast
(Saccharomyces cerevisiae)
Saccharomycetes COX12 30 31
  • 53.81 (n)
OneToMany
Thale Cress
(Arabidopsis thaliana)
eudicotyledons COX6B 30
  • 53.25 (n)
Bread mold
(Neurospora crassa)
Ascomycetes NCU11339 30
  • 62.63 (n)
Fission Yeast
(Schizosaccharomyces pombe)
Schizosaccharomycetes cox12 30
  • 52.26 (n)
Species where no ortholog for COX6B1 was found in the sources mined by GeneCards:
  • Actinobacteria (Mycobacterium tuberculosis)
  • Alicante grape (Vitis vinifera)
  • Alpha proteobacteria (Wolbachia pipientis)
  • Amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • Barley (Hordeum vulgare)
  • Beta proteobacteria (Neisseria meningitidis)
  • Chicken (Gallus gallus)
  • Chromalveolata (Phytophthora infestans)
  • Common water flea (Daphnia pulex)
  • Corn (Zea mays)
  • E. coli (Escherichia coli)
  • Filamentous fungi (Aspergillus nidulans)
  • Firmicute Bacteria (Streptococcus pneumoniae)
  • Green Algae (Chlamydomonas reinhardtii)
  • Honey Bee (Apis mellifera)
  • Loblloly Pine (Pinus taeda)
  • Malaria Parasite (Plasmodium falciparum)
  • Medicago Trunc (Medicago Truncatula)
  • Moss (Physcomitrella patens)
  • Orangutan (Pongo pygmaeus)
  • Pig (Sus scrofa)
  • Rainbow Trout (Oncorhynchus mykiss)
  • Rice (Oryza sativa)
  • Rice Blast Fungus (Magnaporthe grisea)
  • Schistosome Parasite (Schistosoma mansoni)
  • Sea Anemone (Nematostella vectensis)
  • Sea Vase (Ciona intestinalis)
  • Sea Squirt (Ciona savignyi)
  • Sea Urchin (Strongylocentrotus purpuratus)
  • Sorghum (Sorghum bicolor)
  • Soybean (Glycine max)
  • Stem Rust Fungus (Puccinia graminis)
  • Sugarcane (Saccharum officinarum)
  • Tomato (Lycopersicon esculentum)
  • Toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • Wheat (Triticum aestivum)

Evolution for COX6B1 Gene

ENSEMBL:
Gene Tree for COX6B1 (if available)
TreeFam:
Gene Tree for COX6B1 (if available)
Aminode:
Evolutionary constrained regions (ECRs) for COX6B1: view image

Paralogs for COX6B1 Gene

Paralogs for COX6B1 Gene

(1) SIMAP similar genes for COX6B1 Gene using alignment to 2 proteins:

  • CX6B1_HUMAN
  • K7EQD3_HUMAN
genes like me logo Genes that share paralogs with COX6B1: view

Variants for COX6B1 Gene

Sequence variations, with clinical significance, from ClinVar and Humsavar, with links to dbSNP for COX6B1 Gene

SNP ID Clinical significance and condition Chr 19 pos Variation AA Info Type
676113 Benign: not provided 35,651,394(+) G/A INTRON_VARIANT
729622 Likely Benign: not provided 35,651,249(+) G/A SYNONYMOUS_VARIANT
889431 Uncertain Significance: Mitochondrial complex IV deficiency 35,648,373(+) G/A FIVE_PRIME_UTR_VARIANT
889432 Uncertain Significance: Mitochondrial complex IV deficiency 35,651,345(+) C/T SYNONYMOUS_VARIANT
889433 Uncertain Significance: Mitochondrial complex IV deficiency 35,658,598(+) C/T MISSENSE_VARIANT

Additional dbSNP identifiers (rs#s) for COX6B1 Gene

Variation tolerance for COX6B1 Gene

Residual Variation Intolerance Score: 52.8% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 0.12; 2.72% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for COX6B1 Gene

Human Gene Mutation Database (HGMD)
COX6B1
SNPedia medical, phenotypic, and genealogical associations of SNPs for
COX6B1

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot and Structural Variations from Database of Genomic Variants (DGV) for COX6B1 Gene

Disorders for COX6B1 Gene

MalaCards: The human disease database

(9) MalaCards diseases for COX6B1 Gene - From: UniProtKB/Swiss-Prot, OMIM, ClinVar, GTR, Orphanet, DISEASES, and GeneCards

Disorder Aliases PubMed IDs
mitochondrial complex iv deficiency
  • cytochrome c oxidase deficiency
leigh syndrome
  • ls
huntington disease
  • hd
cardiomyopathy, infantile hypertrophic
  • infantile hypertrophic cardiomyopathy
hypertrophic cardiomyopathy
  • familial hypertrophic cardiomyopathy
- elite association - COSMIC cancer census association via MalaCards

UniProtKB/Swiss-Prot

CX6B1_HUMAN
  • Mitochondrial complex IV deficiency (MT-C4D) [MIM:220110]: A disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations, ranging from isolated myopathy to severe multisystem disease affecting several tissues and organs. Features include hypertrophic cardiomyopathy, hepatomegaly and liver dysfunction, hypotonia, muscle weakness, exercise intolerance, developmental delay, delayed motor development and mental retardation. Some affected individuals manifest a fatal hypertrophic cardiomyopathy resulting in neonatal death. A subset of patients manifest Leigh syndrome. {ECO:0000269 PubMed:18499082}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Additional Disease Information for COX6B1

Genetic Association Database
(GAD)
Human Genome Epidemiology Navigator
(HuGE)
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
Open Targets Platform
genes like me logo Genes that share disorders with COX6B1: view

No data available for Genatlas for COX6B1 Gene

Publications for COX6B1 Gene

  1. Nucleotide sequence of the last exon of the gene for human cytochrome c oxidase subunit VIb and its flanking regions. (PMID: 1647217) Taanman JW … De Vries H (Biochimica et biophysica acta 1991) 3 4 23
  2. Human cytochrome c oxidase subunit VIb: characterization and mapping of a multigene family. (PMID: 1651883) Carrero-Valenzuela RD … Forte M (Gene 1991) 3 4 23
  3. Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression. (PMID: 20877624) Hendrickson SL … O'Brien SJ (PloS one 2010) 3 41
  4. Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase. (PMID: 18499082) Massa V … Zeviani M (American journal of human genetics 2008) 3 4
  5. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PMID: 15489334) Gerhard DS … MGC Project Team (Genome research 2004) 3 4

Products for COX6B1 Gene