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

Structure of the gene for the F allele of complement receptor type 1 and sequence of the coding region unique to the S allele.

Journal of immunology (Baltimore, Md. : 1950) - 1 Dec 1993

Vik D P, Wong W W

Abstract excerpt

The genes for human complement receptor type 1 (CR1) F and S alleles have been cloned and span a region of 133-160 kb on chromosome 1. The F allele was found to comprise 39 exons and the S allele contains an additional 8 exons. The leader sequence and 5'-untranslated region are contained in one exon. Each of the long homologous repeats (LHR), which contain seven short consensus repeats (SCR), is composed of 8...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Base Sequence
Share to Molecular Sequence Data

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

Share to Repetitive Sequences, Nucleic Acid

Share to Transcription, Genetic

Source

Identifiers

PMID: 8245463

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

Structure of the gene for the F allele of complement receptor type 1 and sequence of the coding region unique to the S allele.PMID 8245463Read ↗

Structural and functional correlation of the human complement receptor type 1.Semantic proximity Read ↗

Proposed structure of the F' allotype of human CR1. Loss of a C3b binding site may be associated with altered function.Semantic proximity Read ↗

The human complement component C1R gene: the exon-intron structure and the molecular basis of allelic diversity.Semantic proximity Read ↗

Quantitative alleles of CR1: coding sequence analysis and comparison of haplotypes in two ethnic groups.Semantic proximity Read ↗

A polymorphism in the type one complement receptor (CR1) involves an additional cysteine within the C3b/C4b binding domain that inhibits ligand binding.Semantic proximity Read ↗

The murine complement receptor gene family. IV. Alternative splicing of Cr2 gene transcripts predicts two distinct gene products that share homologous domains with both human CR2 and CR1.Semantic proximity Read ↗

Mapping of the domains required for decay acceleration activity of the human factor H‐like protein 1 and factor HSemantic proximity Read ↗

Genomic analysis of the F subtypes of human complement factor B.Semantic proximity Read ↗

The human complement C9 gene: structural analysis of the 5' gene region and genetic polymorphism studies.Semantic proximity Read ↗

Human factor B. Complete cDNA sequence of the BF*S allele.Semantic proximity Read ↗

Mapping of the complement regulatory domains in the human factor H-like protein 1 and in factor H1Semantic proximity Read ↗

Genetic and structural polymorphism of complement receptor 1 in normal Indian subjects.Semantic proximity Read ↗

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