Details for: CYBA
Associated with
Other Information
Genular Protein ID: 1696406250
Symbol: CY24A_HUMAN
Name: Cytochrome b-245 light chain
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 3368442
Title: Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b.
PubMed ID: 3368442
PubMed ID: 15616553
Title: The sequence and analysis of duplication-rich human chromosome 16.
PubMed ID: 15616553
DOI: 10.1038/nature03187
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 2243141
Title: Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
PubMed ID: 2243141
DOI: 10.1172/jci114898
PubMed ID: 2469497
Title: Characterization of two monoclonal antibodies against cytochrome b558 of human neutrophils.
PubMed ID: 2469497
PubMed ID: 12716910
Title: Novel human homologues of p47phox and p67phox participate in activation of superoxide-producing NADPH oxidases.
PubMed ID: 12716910
PubMed ID: 15585859
Title: Site-specific inhibitors of NADPH oxidase activity and structural probes of flavocytochrome b: characterization of six monoclonal antibodies to the p22phox subunit.
PubMed ID: 15585859
PubMed ID: 15561711
Title: Identification of a novel partner of duox: EFP1, a thioredoxin-related protein.
PubMed ID: 15561711
PubMed ID: 15824103
Title: The NADPH oxidase Nox3 constitutively produces superoxide in a p22phox-dependent manner: its regulation by oxidase organizers and activators.
PubMed ID: 15824103
PubMed ID: 15927447
Title: Functional analysis of Nox4 reveals unique characteristics compared to other NADPH oxidases.
PubMed ID: 15927447
PubMed ID: 17140397
Title: Critical roles for p22phox in the structural maturation and subcellular targeting of Nox3.
PubMed ID: 17140397
DOI: 10.1042/bj20060819
PubMed ID: 19948736
Title: Phosphorylation of p22phox on threonine 147 enhances NADPH oxidase activity by promoting p47phox binding.
PubMed ID: 19948736
PubMed ID: 22808130
Title: Molecular interface of S100A8 with cytochrome b and NADPH oxidase activation.
PubMed ID: 22808130
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 16326715
Title: NMR solution structure of the tandem Src homology 3 domains of p47phox complexed with a p22phox-derived proline-rich peptide.
PubMed ID: 16326715
PubMed ID: 1415254
Title: Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).
PubMed ID: 1415254
PubMed ID: 1763037
Title: Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.
PubMed ID: 1763037
PubMed ID: 8168815
Title: Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis.
PubMed ID: 8168815
DOI: 10.1007/bf00201671
PubMed ID: 7964505
Title: 156Pro-->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox.
PubMed ID: 7964505
PubMed ID: 10910929
Title: Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox).
PubMed ID: 10910929
PubMed ID: 10759707
Title: Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients.
PubMed ID: 10759707
PubMed ID: 10914676
Title: Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiency.
PubMed ID: 10914676
PubMed ID: 18422995
Title: Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease.
PubMed ID: 18422995
PubMed ID: 19388116
Title: Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generation.
PubMed ID: 19388116
DOI: 10.1002/humu.21029
PubMed ID: 23910690
Title: Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients.
PubMed ID: 23910690
Sequence Information:
- Length: 195
- Mass: 21013
- Checksum: 428427AD19398240
- Sequence:
MGQIEWAMWA NEQALASGLI LITGGIVATA GRFTQWYFGA YSIVAGVFVC LLEYPRGKRK KGSTMERWGQ KYMTAVVKLF GPFTRNYYVR AVLHLLLSVP AGFLLATILG TACLAIASGI YLLAAVRGEQ WTPIEPKPRE RPQIGGTIKQ PPSNPPPRPP AEARKKPSEE EAAVAAGGPP GGPQVNPIPV TDEVV
Genular Protein ID: 633215633
Symbol: H3BNP7_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 15616553
Title: The sequence and analysis of duplication-rich human chromosome 16.
PubMed ID: 15616553
DOI: 10.1038/nature03187
Sequence Information:
- Length: 210
- Mass: 22827
- Checksum: 6E1F507E8B24CDB9
- Sequence:
MGQIEWAMWA NEQALASGLI LITGGIVATA GRFTQWYFGA YSIVAGVFVC LLEYPRGKRK KGSTMERWGQ KYMTAVVKLF GPFTRNYYVR AVLHLLLSVP AGFLLATILG TACLAIASGI YLLSQVPPAR RGNCPPLAVR LLVCVRGKGA ALSVYAFRVW KWSSVSSLTD LPPAELSFRT PSCCQVLIWA VALFSGGHPH PPRLPAATHS
Genular Protein ID: 4020219498
Symbol: B4DT46_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 131
- Mass: 14019
- Checksum: 0F8AF47330762B7F
- Sequence:
MERWGQKHMT AVVKLFGPFT RNYYVRAVLH LLLSVPAGFL LATILGTACL AIASGIYLLA AVRGEQWTPI EPKPRERPQI GGTIKQPPSN PPPRPPAEAR KKPSEEEAAV AAGGPPGGPQ VNPIPVTDEV V
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.