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

Linkage of the gene for equine combined immunodeficiency disease to microsatellite markers HTG8 and HTG4; synteny and FISH mapping to ECA9.

Animal genetics - 1 Aug 1997

Bailey E, Reid R C, Skow L C, Mathiason K, Lear T L, McGuire T C

Abstract excerpt

Equine combined immunodeficiency disease (CID) is caused by homozygosity for an autosomal recessive gene. To identify linked markers for the disease, we studied a family segregating for the equine CID gene. A stallion and 19 of his CID-affected offspring were tested for marker segregation at 23 microsatellite DNA loci. His CID-affected offspring inherited only one of his two alleles at the HTG8 and HTG4 loci,...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Chromosome Mapping
Share to Genetic Linkage

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

Share to Hybrid Cells

Share to In Situ Hybridization, Fluorescence

Share to Linkage Disequilibrium

Share to Microsatellite Repeats

Source

Identifiers

PMID: 9345723
DOI: 10.1111/j.1365-2052.1997.00152.x

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.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Linkage of the gene for equine combined immunodeficiency disease to microsatellite markers HTG8 and HTG4; synteny and FISH mapping to ECA9.PMID 9345723Read ↗

Genetical and physical assignments of equine microsatellites--first integration of anchored markers in horse genome mapping.Semantic proximity Read ↗

A genetic linkage map of microsatellites in the domestic cat (Felis catus).Semantic proximity Read ↗

Genome-Wide Association Study and Subsequent Exclusion of ATCAY as a Candidate Gene Involved in Equine Neuroaxonal Dystrophy Using Two Animal Models.Semantic proximity Read ↗

Mapping of equine cerebellar abiotrophy to ECA2 and identification of a potential causative mutation affecting expression of MUTYH.Semantic proximity Read ↗

Isolation, characterization and FISH assignments of horse BAC clones containing type I and II markers.Semantic proximity Read ↗

Molecular characterization of the equine collagen, type IX, alpha 2 (COL9A2) gene on horse chromosome 2p16-->p15.Semantic proximity Read ↗

Six new cosmid derived and physically mapped equine dinucleotide repeat microsatellites.Semantic proximity Read ↗

The Complete Map of the Ig Heavy Chain Constant Gene Region Reveals Evidence for Seven IgG Isotypes and for IgD in the HorseSemantic proximity Read ↗

Characterization and RH mapping of six gene-associated equine microsatellite markers.Semantic proximity Read ↗

Mapping of equine potassium chloride co-transporter (SLC12A4) and amino acid transporter (SLC7A10) and preliminary studies on associations between SNPs from SLC12A4, SLC7A10 and SLC7A9 and osmotic fragility of erythrocytes.Semantic proximity Read ↗

A kinase-negative mutation of DNA-PK(CS) in equine SCID results in defective coding and signal joint formation.Semantic proximity Read ↗

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