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

Homologous pigmentation mutations in human, mouse and other model organisms.

Human molecular genetics - 1 Jan 1997

Jackson I J

Abstract excerpt

Mouse coat colour genes have long been studied as a paradigm for genetic interactions in development. A number of these genes have been cloned and most correspond to human genetic disease loci. The proteins encoded by these genes include transcription factors, receptor tyrosine kinases and growth factors, G-protein coupled receptors and their ligands, membrane proteins, structural proteins and enzymes. Many of...

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 Genetic Diseases, Inborn
Share to Genetic Variation

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

Share to Molecular Sequence Data

Share to Mutation

Share to Proteins

Share to Sequence Alignment

Source

Identifiers

PMID: 9300652
DOI: 10.1093/hmg/6.10.1613

Genes

LYST

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

Homologous pigmentation mutations in human, mouse and other model organisms.PMID 9300652Read ↗

The color loci of mice--a genetic century.Semantic proximity Read ↗

Mouse coat colour mutations: a molecular genetic resource which spans the centuries.Semantic proximity Read ↗

Nomenclature for identified pigmentation genes in the mouse.Semantic proximity Read ↗

Human pigmentation genes: identification, structure and consequences of polymorphic variation.Semantic proximity Read ↗

Iris phenotypes and pigment dispersion caused by genes influencing pigmentation.Semantic proximity Read ↗

Mouse coat color mutations: from fancy mice to functional genomics.Semantic proximity Read ↗

Genetic disorders of pigmentation.Semantic proximity Read ↗

Pleiotropic effects of coat colour-associated mutations in humans, mice and other mammals.Semantic proximity Read ↗

The etiology and molecular genetics of human pigmentation disordersSemantic proximity Read ↗

The developmental biology of melanocytes and its application to understanding human congenital disorders of pigmentation.Semantic proximity Read ↗

Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders.Semantic proximity Read ↗

Monogenic pigmentary skin disorders: genetics and pathophysiology.Semantic proximity Read ↗

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