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Membrane-Associated Transporter Protein

Known as: Melanoma Antigen AIM1, SLC45A2, Protein AIM-1 
Membrane-associated transporter protein (530 aa, ~58 kDa) is encoded by the human SLC45A2 gene. This protein is involved in the modulation of both… 
National Institutes of Health

Related topics

Related topics

12 relations
Cell Differentiation processCellular MembraneIntegral Membrane ProteinsLigand Binding

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Analysis of Positive Selection at Single Nucleotide Polymorphisms Associated with Body Mass Index Does Not Support the "Thrifty Gene" Hypothesis.
Highly Cited
2015
Highly Cited
2015
Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data
To characterize natural selection, various analytical methods for detecting candidate genomic regions have been developed. We… 
Highly Cited
2013
Highly Cited
2013
The Genetic Basis of White Tigers
Highly Cited
2013
Highly Cited
2013
Slc45a2 and V‐ATPase are regulators of melanosomal pH homeostasis in zebrafish, providing a mechanism for human pigment evolution and disease
We present here the positional cloning of the Danio rerio albino mutant and show that the affected gene encodes Slc45a2. The… 
Highly Cited
2013
Highly Cited
2013
Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.
Oculocutaneous albinism (OCA) is a heterogeneous and autosomal recessive disorder with hypopigmentation in the eye, hair, and… 
Highly Cited
2013
Highly Cited
2013
Improved eye- and skin-color prediction based on 8 SNPs
Aim To improve the 7-plex system to predict eye and skin color by increasing precision and detailed phenotypic descriptions… 
Highly Cited
2008
Highly Cited
2008
SLC45A2: a novel malignant melanoma‐associated gene
Human pigmentation appears to be one of the strongest risk factors for malignant melanoma (MM). In humans, there is a long list… 
Highly Cited
2008
Highly Cited
2008
Comprehensive analysis of oculocutaneous albinism among non-Hispanic caucasians shows that OCA1 is the most prevalent OCA type.
Oculocutaneous albinism (OCA) is a genetically heterogeneous group of disorders characterized by absent or reduced pigmentation… 
Highly Cited
1990
Highly Cited
1990
Genome imprinting phenomena on mouse chromosome 7.
Heterozygotes for the reciprocal translocation T(7;15)9H were intercrossed, with albino (c) and underwhite (uw) as genetic… 
Highly Cited
1981
Highly Cited
1981
Progressive ankylosis, a new skeletal mutation in the mouse.
Progressive ankylosis, ank, a new recessive skeletal mutation causing a noninflammatory joint disease in mice is described… 
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