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      <title>My dazzling padlet by DOLORES HO SYN XIAN</title>
      <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7</link>
      <description>Made with good vibes</description>
      <language>en-us</language>
      <pubDate>2022-05-30 15:30:09 UTC</pubDate>
      <lastBuildDate>2025-12-14 02:59:23 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
      <image>
         <url></url>
      </image>
      <item>
         <title>Non-Mendelian Genetics </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204806100</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:30:52 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204806100</guid>
      </item>
      <item>
         <title>1. Co-dominance </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204808324</link>
         <description><![CDATA[<div>a type of inheritance in which two alleles of the same gene are expressed separately to yield different traits in an individual </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:33:12 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204808324</guid>
      </item>
      <item>
         <title>Phenotypic Ratio </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204809793</link>
         <description><![CDATA[<div>phenotypic ratio of F2 generation <br><strong>1 : 2 : 1&nbsp;</strong></div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:34:58 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204809793</guid>
      </item>
      <item>
         <title>Examples </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204813729</link>
         <description><![CDATA[<div>parents: pure breed white cow x pure breed red cow<br>&nbsp;|&nbsp; &nbsp; &nbsp; &nbsp; |&nbsp; &nbsp; &nbsp;CR&nbsp; &nbsp; | CR<br>&nbsp;| CW | CR CW | CR CW<br>&nbsp;| CW | CR CW | CR CW<br><br>F1 generation: all offspring = roan cow<br><br>&nbsp;|&nbsp; &nbsp; &nbsp; &nbsp;|&nbsp; &nbsp; CR&nbsp; &nbsp; | CW<br>&nbsp;| CR | CR CR | CR CW<br>&nbsp;| CW | CR CW | CW CW<br><br>F2 generation: 1 white : 2 roan : 1 red</div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:39:08 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204813729</guid>
      </item>
      <item>
         <title>2. Incomplete dominance </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204815410</link>
         <description><![CDATA[<div>a form of gene interaction in which both alleles of a gene at a locus are partially expressed<br>- often resulting in an intermediate or different phenotype&nbsp;</div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:41:10 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204815410</guid>
      </item>
      <item>
         <title>Phenotypic Ratio </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204816343</link>
         <description><![CDATA[<div>phenotypic ratio of F2 generation <br><strong>1 : 2 : 1</strong></div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:42:23 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204816343</guid>
      </item>
      <item>
         <title>Example</title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204817853</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1541196740/0c78d9b43164a511f04705ef243c3d60/image.png" />
         <pubDate>2022-05-30 15:44:16 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204817853</guid>
      </item>
      <item>
         <title>3. Order of Dominance (multiple alleles) </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204820803</link>
         <description><![CDATA[<div>dominance is the phenomenon of one allele of a gene on a chromosome masking or overriding the effect of a different allele of the same gene on the other copy of the chromosome </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:47:36 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204820803</guid>
      </item>
      <item>
         <title>Example </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204824950</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1541196740/3baa00335749e996a49ef31410e0fd1a/image.png" />
         <pubDate>2022-05-30 15:52:17 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204824950</guid>
      </item>
      <item>
         <title>4. Lethal alleles </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204826359</link>
         <description><![CDATA[<div>alleles that cause an organism to die only when present in a homozygous condition </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:53:56 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204826359</guid>
      </item>
      <item>
         <title>Phenotypic ratio </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204828681</link>
         <description><![CDATA[<div>when cross between 2 mice heterozygous for coat colour gene&nbsp;<br>expected - 3 (75%) : 1 (25%)&nbsp;<br>however dominant genotype is lethal&nbsp;<br>ratio - 2/3 (heterozygous) : 1/3 (recessive) </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 15:56:41 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204828681</guid>
      </item>
      <item>
         <title>Example </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204833486</link>
         <description><![CDATA[<div>Manx cat (mutated) - M^L gene <br><strong>expected ratio</strong> - 1 (homozygous) : 2 (heterozygous) : 1 (recessive) <br>double copy of M^L alleles = lethal <br><strong>observed ratio</strong> - 2/3 Manx cat : 1/3 normal cat<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 16:00:51 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204833486</guid>
      </item>
      <item>
         <title>5. Pleiotropy </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204852432</link>
         <description><![CDATA[<div>phenomenon in which a single locus affects two or more apparently unrelated phenotypic traits </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 16:21:42 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204852432</guid>
      </item>
      <item>
         <title>Examples </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204856011</link>
         <description><![CDATA[<div>sickle cell anemia, Marfan syndrome, porphyria, and PKU are caused by mutations in a single gene (a different gene for each disease) but have multiple effects all over the body&nbsp;<br><br>Marfan syndrome&nbsp;<br>- single gene for fibrillin on chromosome 15&nbsp;<br>- inherited disorder of the connective tissue that cause abnormalities of the patient's eye, cardiovascular system, and musculoskeletal system </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 16:25:44 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204856011</guid>
      </item>
      <item>
         <title>6. Gene Interaction </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204936799</link>
         <description><![CDATA[<div>the set of functional association between genes&nbsp;<br><br>a trait may need interaction between multiple genes -&gt; more than one gene is responsible for the phenotype of the trait </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 18:03:27 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204936799</guid>
      </item>
      <item>
         <title>Epistasis </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204938144</link>
         <description><![CDATA[<div>occurs in:&nbsp;<br>1. whenever two or more loci interact to create new phenotypes&nbsp;<br>2. whenever an allele at one locus masks the effects of alleles at one or more other loci<br>3. whenever an allele at one locus modifies the effects or alleles at one or more other loci </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 18:05:13 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204938144</guid>
      </item>
      <item>
         <title>Example </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204941013</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1541196740/a177a9a51d71b72ab254ab7adab59a8d/image.png" />
         <pubDate>2022-05-30 18:08:46 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204941013</guid>
      </item>
      <item>
         <title>Example </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204945632</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1541196740/12d94ca290491314a471dc2784191826/image.png" />
         <pubDate>2022-05-30 18:14:31 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204945632</guid>
      </item>
      <item>
         <title></title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204946799</link>
         <description><![CDATA[<div>precursor -&gt; intermediate -&gt; final product </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 18:16:09 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204946799</guid>
      </item>
      <item>
         <title>7. Polygenic Inheritance </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204949488</link>
         <description><![CDATA[<div>quantitative inheritance, where multiple independent genes have an additive or similar effect on a single quantitative trait&nbsp;</div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1541196740/d820bf4c3270909cd973fb7995c95af6/image.png" />
         <pubDate>2022-05-30 18:19:37 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204949488</guid>
      </item>
      <item>
         <title>Variations </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204952309</link>
         <description><![CDATA[<div>discontinuous variation - characteristics fall into distinct groups (sometimes 2 forms of a characteristic)&nbsp;<br>e.g. blood group, attached/detached earlobes, etc<br><br>continuous variation - characteristics which do not show clear cut differences (show a range of differences)<br>e.g. height, weight, eye colour, etc</div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 18:23:26 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204952309</guid>
      </item>
      <item>
         <title>Predictions Polygenic Inheritance</title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204953470</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1541196740/f503281e6a1b7f7df2df1a28e198dd28/image.png" />
         <pubDate>2022-05-30 18:25:01 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204953470</guid>
      </item>
      <item>
         <title>Predictions Polygenic Inheritance </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204954794</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1541196740/c248bfda2e2c1bc5b8ede3ba8e6913c4/image.png" />
         <pubDate>2022-05-30 18:26:43 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204954794</guid>
      </item>
      <item>
         <title>8. Linked Genes </title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204956156</link>
         <description><![CDATA[<div>genes that are likely to be inherited together because they are physically close to one another on the same chromosome&nbsp;<br>more likely inherit together = breaking law of independent assortment <br><br></div>]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1541196740/8961388c3e15ef9ec0fa8f78f8a58c5b/image.png" />
         <pubDate>2022-05-30 18:28:39 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204956156</guid>
      </item>
      <item>
         <title>Gene Map</title>
         <author>21009838_2</author>
         <link>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204964429</link>
         <description><![CDATA[<div>steps to determine the distance between genes on the chromosome:&nbsp;<br>1. find out whether it is autosomal or sex-linked&nbsp;<br>&nbsp; &nbsp;- autosomal = affects both gender equally<br>&nbsp; &nbsp;- sex-linked = gender biased, affects one gender<br>2. choose an autosomal with know mutation&nbsp;<br>&nbsp; &nbsp;- parents (wild type and double mutant) cross to form F1&nbsp;<br>&nbsp; &nbsp;- F1 self to form F2 = determine whether it is linked or not<br>3. test cross (if it is linked - not 9 : 3 : 3 : 1 ratio)&nbsp;<br>&nbsp; &nbsp; - F1 cross double mutant to form F2<br>&nbsp; &nbsp; - F2 = determine whether it is linked or not, not 1 : 1 : 1 : 1\<br>&nbsp; &nbsp; - use recombinant frequency to find the cM/distance of the gene<br>4. redo step 3 with a different gene (on the same chromosome)<br>     - pinpointing frequency = more accurate, can tell the estimation of where exactly the gene is located </div>]]></description>
         <enclosure url="" />
         <pubDate>2022-05-30 18:39:31 UTC</pubDate>
         <guid>https://padlet.com/21009838_2/brw8xi9gcsrosyj7/wish/2204964429</guid>
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