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

Topics Community

Article

A missense mutation in ASIP is associated with light point variation in donkeys.

Animal genetics - 1 Aug 2020

Yu Yan, Shang Songyang, Zhang Xiaoying, Wang Zhe, Dang Wanyi, Zhang Junpeng, Zhu Yanxu, Dang Ruihua, Irwin David M, Zhang Shuyi

Abstract excerpt

No abstract is available from the source.

Topics

Agouti Signaling Protein
Animal Fur
Animals
Equidae
Mutation, Missense
Phenotype

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32311147
DOI: 10.1111/age.12940

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A missense mutation in ASIP is associated with light point variation in donkeys.PMID 32311147Read ↗

Validation of a candidate causative mutation for white spotting in donkeys.Semantic proximity Read ↗

ASIP gene variation in Chinese donkeys.Semantic proximity Read ↗

A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys.Semantic proximity Read ↗

Evidence supports white spotting in donkeys as a homozygous lethal condition.Semantic proximity Read ↗

SPOTTING VARIATIONS IN THE LEOPARD FROG. A TEST FOR THE GENETIC BASIS IN THE RANA PIPIENS "BURNSI" VARIANT.Semantic proximity Read ↗

Single base-pair deletion in ASIP exon 3 associated with recessive black phenotype in impala (Aepyceros melampus).Semantic proximity Read ↗

The albinism of the feral Asinara white donkeys (Equus asinus) is determined by a missense mutation in a highly conserved position of the tyrosinase (TYR) gene deduced protein.Semantic proximity Read ↗

A de novo missense mutation in KIT is responsible for dominant white spotting phenotype in a Standardbred horse.Semantic proximity Read ↗

The b(c) allele of TYRP1 is causative for the recessive brown (liver) colour in German Shepherd dogs.Semantic proximity Read ↗

TYRP1:c.555T>G is a recurrent mutation found in Australian Shepherd and Miniature American Shepherd dogs.Semantic proximity Read ↗

A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosisSemantic proximity Read ↗

Characterization of different 5'-untranslated exons of the ASIP gene in black-and-tan Doberman Pinscher and brindle Boxer dogs.Semantic proximity Read ↗

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