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Skin Pigmentation and Familial Melanoma​​ - Home

This page was produced as an assignment for Genetics 564 , an undergraduate course at the University of Wisconsin-Madison. 

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Skin Pigmentation and Familial Melanoma​​ - Home | busalacchigen564s16.weebly.com Reviews
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This page was produced as an assignment for Genetics 564 , an undergraduate course at the University of Wisconsin-Madison. 
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1 protein
2 homology
3 phylogeny
4 ontology
5 domains
6 interaction network
7 specific aims
8 conclusions
9 mc1r gene
10 dr n davis
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protein,homology,phylogeny,ontology,domains,interaction network,specific aims,conclusions,mc1r gene,dr n davis,what is melanoma,symptoms and treatment,matthew busalacchi,mbusalacchi@wisc edu,wwwgenetics564 weebly com,website visitors,references,images
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Skin Pigmentation and Familial Melanoma​​ - Home | busalacchigen564s16.weebly.com Reviews

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This page was produced as an assignment for Genetics 564 , an undergraduate course at the University of Wisconsin-Madison. 

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Specific AIMS - Skin Pigmentation and Familial Melanoma​​

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Skin Pigmentation and Familial Melanoma. 8203; Identification of MC1R protein function in regulation of pigment production. Familial melanoma is characterized by large, flat, asymmetric, and different colored moles on the surface of the skin.1 One gene associated with familial melanoma is the. Melanocortin 1 receptor (MC1R). The role of the MC1R protein is still unknown in the signaling pathway that leads to pigmentation and cell proliferation. Obtain sequences of the trumpetfish genome that were produce...

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Protein - Skin Pigmentation and Familial Melanoma​​

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Skin Pigmentation and Familial Melanoma. Which area of the MC1R protein interests you? In this section, you will learn about the many homologous organisms that have the MC1R protein. Here, you will learn all about the phylogeny and the history of the MC1R protein. In this section, we will discuss the biological process, molecular function, and cellular component of the MC1R protein. In this section, you will gain an understanding of the portions of the protein that have a meaning to its function.

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Domains - Skin Pigmentation and Familial Melanoma​​

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Skin Pigmentation and Familial Melanoma. What are protein domains? Protein domains are regions of a particular protein that are associated with a function of the protein or a structural aspect of the protein [1]. Most commonly, the domains of the protein involve a part of the gene ontology that we discussed earlier [2]. This type of analysis allows researchers to determine facts regarding the evolution of the protein as well. What domains lie within MC1R? What are protein domains? Create a free website.

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Conclusions - Skin Pigmentation and Familial Melanoma​​

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Skin Pigmentation and Familial Melanoma. We will discuss the role of the MC1R protein, as well as the conservation of the protein across varies species. Originally, we believed that the MC1R protein acted as a switch and either produced pheomelanin (lighter pigment) or eumelanin (darker pigment) in species. We discovered that there may also be a mix of colors that occur within the body that produce a little of each color. Our hypothesis is that the MC1R protein plays an integral role in regulating the si...

5

Interaction Network - Skin Pigmentation and Familial Melanoma​​

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Skin Pigmentation and Familial Melanoma. What is a protein interaction network? A protein interaction network allows us to visualize the many proteins that may interact or have been known to interact with a particular protein. The network allows us to categorize similar proteins that are involved in a similar process within the organism. By understanding this information, we are able to determine with proteins we may do further research with in the future. What proteins are interact with MC1R?

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Projects - Genetics 564

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Spring 2016 Student Projects. Matthew Busalacchi: Familial Melanoma and Pigmentation (MC1R). Salvador Carranza: Cystinosis (CTNS). Mikayla Gallenberger: Acute Lymphoblastic Leukemia (PAX5). Sara Grange: Synesthesia (KIAA0319). Aidan Holmes: Wilson Disease (ATP7B). Bailey Marquardt: Developmental Dyslexia (ROBO1). Troy Meikle: Autoimmune lymphoproliferative syndrome (FAS). Mary Mohr: Cardiovascular Disease in Women (BCAR1/p130CAS). Kathryn Ness: CHARGE Syndrome (CHD7). Tia Ramirez: FOXG1 Syndrome (FOXG1).

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