CD177 (human) _ Clone MEM_166
- Known as:
- CD177 (H. sapiens) _ Clone MEM_166
- Catalog number:
- T-1374.0100
- Product Quantity:
- 100ìg
- Category:
- -
- Supplier:
- New Immunology
- Gene target:
- CD177 (human) _ Clone MEM_166
Related genes to: CD177 (human) _ Clone MEM_166
- Gene:
- CD177 NIH gene
- Name:
- CD177 molecule
- Previous symbol:
- -
- Synonyms:
- PRV1, HNA2A, NB1
- Chromosome:
- 19q13.31
- Locus Type:
- gene with protein product
- Date approved:
- 2005-08-12
- Date modifiied:
- 2015-08-27
- Gene:
- CD177P1 NIH gene
- Name:
- CD177 molecule pseudogene 1
- Previous symbol:
- CD177P
- Synonyms:
- -
- Chromosome:
- 19q13.31
- Locus Type:
- pseudogene
- Date approved:
- 2008-08-06
- Date modifiied:
- 2016-03-24
- Gene:
- EVA1A NIH gene
- Name:
- eva-1 homolog A, regulator of programmed cell death
- Previous symbol:
- TMEM166, FAM176A
- Synonyms:
- FLJ13391
- Chromosome:
- 2p12
- Locus Type:
- gene with protein product
- Date approved:
- 2006-07-26
- Date modifiied:
- 2016-02-15
Related products to: CD177 (human) _ Clone MEM_166
Related articles to: CD177 (human) _ Clone MEM_166
- Most humans harbor both CD177neg and CD177pos neutrophils but 1-10% of people are CD177null, placing them at risk for formation of anti-neutrophil antibodies that can cause transfusion-related acute lung injury and neonatal alloimmune neutropenia. By deep sequencing the CD177 locus, we catalogued CD177 single nucleotide variants and identified a novel stop codon in CD177null individuals arising from a single base substitution in exon 7. This is not a mutation in CD177 itself, rather the CD177null phenotype arises when exon 7 of CD177 is supplied entirely by the CD177 pseudogene (CD177P1), which appears to have resulted from allelic gene conversion. In CD177 expressing individuals the CD177 locus contains both CD177P1 and CD177 sequences. The proportion of CD177hi neutrophils in the blood is a heritable trait. Abundance of CD177hi neutrophils correlates with homozygosity for CD177 reference allele, while heterozygosity for ectopic CD177P1 gene conversion correlates with increased CD177neg neutrophils, in which both CD177P1 partially incorporated allele and paired intact CD177 allele are transcribed. Human neutrophil heterogeneity for CD177 expression arises by ectopic allelic conversion. Resolution of the genetic basis of CD177null phenotype identifies a method for screening for individuals at risk of CD177 isoimmunisation. - Source: PubMed
Publication date: 2016/05/26
Wu ZuopengLiang RongOhnesorg ThomasCho VickyLam WesleyAbhayaratna Walter PGatenby Paul APerera ChandimaZhang YafeiWhittle BelindaSinclair AndrewGoodnow Christopher CField MatthewAndrews T DanielCook Matthew C