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 basis of the Kell (K1) phenotype.

Blood - 15 Feb 1995

Lee S, Wu X, Reid M, Zelinski T, Redman C

Abstract excerpt

K1 (K, Kell) is a strong immunogen; its antibodies can cause severe reactions if incompatible blood is transfused and may cause hemolytic disease of the newborn in sensitized mothers. K1 is a member of the Kell blood group system, which is complex, containing over 20 different antigens. Some of the antigens are organized in allelic pairs of high and low prevalence whereas others are independently expressed. K1,...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Base Sequence
Share to DNA

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Genotype

Share to Molecular Sequence Data

Share to Phenotype

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 7849312

Genes

KEL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular basis of the Kell (K1) phenotype.PMID 7849312Read ↗

A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen.Semantic proximity Read ↗

A novel KEL*1,3 allele with weak Kell antigen expression confirming the cis-modifier effect of KEL3.Semantic proximity Read ↗

KEL*02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,-2 phenotypes.Semantic proximity Read ↗

Genotyping of KEL1 and KEL2 of the human Kell blood group system by the polymerase chain reaction with sequence-specific primers.Semantic proximity Read ↗

Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull ) phenotypes.Semantic proximity Read ↗

Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American.Semantic proximity Read ↗

The Kell blood group system.Semantic proximity Read ↗

Molecular basis of Kell blood group phenotypes.Semantic proximity Read ↗

The Kell blood group system: Kell and XK membrane proteins.Semantic proximity Read ↗

Another example of a KEL1 variant red cell phenotype due to a threonine to serine change at position 193 of Kell glycoprotein.Semantic proximity Read ↗

Molecular basis of two novel and related high-prevalence antigens in the Kell blood group system, KUCI and KANT, and their serologic and spatial association with K11 and KETI.Semantic proximity Read ↗

Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles.Semantic proximity Read ↗

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