Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Molecular genetic analysis of the Jk(a-b-) phenotype in Chinese: A novel silent recessive JK allele.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis - 1 Apr 2016

Zhang Ai, Chi Quan, Lin Hongkeng, She Yimin

Abstract excerpt

The Jk(a-b-) phenotype, referred to as Jknull, is rare in most populations. This blood type is characterized by the absence of Kidd glycoprotein on the surface of red blood cells (RBCs) and moderately reduced ability to concentrate urine. The molecular basis for Jknull phenotype includes splice-s...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Asian People
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Recessive

Share to Membrane Transport Proteins

Source

Identifiers

PMID: 26969102
DOI: 10.1016/j.transci.2015.04.014

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-26969102-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular genetic analysis of the Jk(a-b-) phenotype in Chinese: A novel silent recessive JK allele.PMID 26969102Read ↗

The mutation spectrum of the JK-null phenotype in the Chinese population.Semantic proximity Read ↗

Erythroid urea transporter deficiency due to novel JKnull alleles.Semantic proximity Read ↗

A novel mutation at the JK locus causing Jk null phenotype in a Chinese family.Semantic proximity Read ↗

Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families.Semantic proximity Read ↗

A novel missense mutation nt737T>G of JK gene with Jk(a-b-) phenotype in Chinese blood donors.Semantic proximity Read ↗

JK null alleles identified from Japanese individuals with Jk(a−b−) phenotype.Semantic proximity Read ↗

A Caucasian JK*A/JK*B woman with Jk(a+b-) red blood cells, anti-Jkb, and a novel JK*B allele c.1038delG.Semantic proximity Read ↗

Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns.Semantic proximity Read ↗

A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a-b-) probands from Guam.Semantic proximity Read ↗

Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors.Semantic proximity Read ↗

Kidd blood group system: a reviewSemantic proximity Read ↗

Novel JK*01 allele with c.299C>T p.(Thr100Ile) single nucleotide variant associated with loss of Jka expression in two African American donors.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.