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

Genomic structure of the human unconventional myosin VI gene.

Gene - 31 Dec 2000

Ahituv N, Sobe T, Robertson N G, Morton C C, Taggart R T, Avraham K B

Abstract excerpt

Mutations in myosin VI (Myo6) cause deafness and vestibular dysfunction in Snell's waltzer mice. Mutations in two other unconventional myosins cause deafness in both humans and mice, making myosin VI an attractive candidate for human deafness. In this report, we refined the map position of human...

Read the complete abstract on PubMed

Topics

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

Share to Deafness
Share to Family Health
Share to Fetus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Introns

Share to Myosin Heavy Chains

Share to Point Mutation

Share to Polymorphism, Single-Stranded Conformational

Source

Identifiers

PMID: 11167014
DOI: 10.1016/s0378-1119(00)00535-7

Genes

MYO6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-11167014-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genomic structure of the human unconventional myosin VI gene.PMID 11167014Read ↗

Targeted Next-Generation Sequencing Analysis Reveals a Novel Genetic Variant in MYO6 Gene in an Indian Family with Postlingual Nonsyndromic Hearing Loss.Semantic proximity Read ↗

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.Semantic proximity Read ↗

Research Progress of MYO6 Variant-Associated Hereditary Hearing Loss.Semantic proximity Read ↗

Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing.Semantic proximity Read ↗

Mutations of MYO6 are associated with recessive deafness, DFNB37.Semantic proximity Read ↗

Unconventional myosins and the genetics of hearing loss.Semantic proximity Read ↗

Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction.Semantic proximity Read ↗

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.Semantic proximity Read ↗

A Novel ENU-Induced Mutation in Myo6 Causes Vestibular Dysfunction and Deafness.Semantic proximity Read ↗

Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity.Semantic proximity Read ↗

Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.Semantic proximity Read ↗

Defective myosin VIIA gene responsible for Usher syndrome type 1B.Semantic proximity Read ↗

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