Varaico: Literature-Extracted Genetic Variants

Gene:TYRP1
Variant:p.S166*
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TYRP1

NM_000550.3:p.S166*

Associated Papers

Undiagnosed disease program in South Africa: Results from first 100 exomes.

Moosa S et al.

American Journal of Medical Genetics. Part A, 2022

Common and Founder Mutations for Monogenic Traits in Sub-Saharan African Populations.

Krause A et al.

Annual Review of Genomics and Human Genetics, 2018

A large insertion in intron 2 of the TYRP1 gene associated with American Palomino phenotype in American mink.

Cirera S et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society, 2016

The brown coat colour of Coppernecked goats is associated with a non-synonymous variant at the TYRP1 locus on chromosome 8.

Becker D et al.

Animal Genetics, 2015

A dominant mutation in tyrp1A leads to melanophore death in zebrafish.

Krauss J et al.

Pigment Cell & Melanoma Research, 2014

Melanesian blond hair is caused by an amino acid change in TYRP1.

Kenny EE et al.

Science (new York, N.y.), 2012

Oculocutaneous albinism type 3: a Japanese girl with novel mutations in TYRP1 gene.

Yamada M et al.

Journal of Dermatological Science, 2011

Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism.

Forshew T et al.

Clinical Genetics, 2005

Oculocutaneous albinism types 1 and 3 are ER retention diseases: mutation of tyrosinase or Tyrp1 can affect the processing of both mutant and wild-type proteins.

Toyofuku K et al.

Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2001

Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa.

Kerr R et al.

Human Mutation, 2000

Albinism.

Oetting WS

Current Opinion in Pediatrics, 1999

Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism.

Oetting WS et al.

Human Mutation, 1999

Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.

Manga P et al.

American Journal of Human Genetics, 1997

The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.

Kedda MA et al.

American Journal of Human Genetics, 1994

Allelism in human oculocutaneous albinism.

Warren ST

American Journal of Human Genetics, 1981

Tyrosinase and tyrosinase related protein 1 alleles specify domestic cat coat color phenotypes of the albino and brown loci.

Schmidt-Küntzel A et al.

The Journal of Heredity, 0

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