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      <title>My smart wall: Genetics by Poonam Singhal</title>
      <link>https://padlet.com/poonam_singhal/genetics</link>
      <description>Made by Ms Poonam Singhal</description>
      <language>en-us</language>
      <pubDate>2017-08-08 13:57:03 UTC</pubDate>
      <lastBuildDate>2023-02-21 19:23:24 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>Gene</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451505</link>
         <description><![CDATA[<div>A section of DNA, that codes for a particular protein <br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:33:42 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451505</guid>
      </item>
      <item>
         <title>Gene pool</title>
         <author>ananya_lunkad1</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451507</link>
         <description><![CDATA[<div>Definition: The stock of different genes in an interbreeding population.<br><br>The sum total of genes of all individuals of a genetic population constitute the gene pool</div>]]></description>
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         <pubDate>2017-08-09 05:33:44 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451507</guid>
      </item>
      <item>
         <title>Allele</title>
         <author>nandan_venkatesan</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451510</link>
         <description><![CDATA[<div>Two different forms of the same gene </div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:33:48 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451510</guid>
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      <item>
         <title>Gene Mutation</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451517</link>
         <description><![CDATA[<div>A <strong>gene mutation </strong>is a change in the nucleotide sequence of a section of DNA coding for a specific trait.<br><br>All creds to BioNinja<br><br></div><div><br></div><div><br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:33:59 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451517</guid>
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      <item>
         <title>Silent Mutation</title>
         <author>nandan_venkatesan</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451519</link>
         <description><![CDATA[<div>mutations that don't significantly alter the phenotype of the organism<br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:34:01 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451519</guid>
      </item>
      <item>
         <title>Genotype </title>
         <author>shania_sharma</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451533</link>
         <description><![CDATA[<div>The genetic makeup of a certain trait which is responsible for the phenotype. </div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:34:26 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451533</guid>
      </item>
      <item>
         <title>Substitution mutations</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451543</link>
         <description><![CDATA[<div>A type of point mutation in which a single nucleotide is substituted with a different nucleotide that may result in an altered sequence of amino acid during translation, which may render the newly synthesized protein ineffective.<br>(Exchanges one base for another</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:34:44 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451543</guid>
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      <item>
         <title>Dominant Allele</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451545</link>
         <description><![CDATA[<div>Dominant alleles show their effect even if the individual only has one copy of the allele (also known as being heterozygous). For example, the allele for brown eyes is dominant, therefore you only need one copy of the 'brown eye' allele to have brown eyes (although, with two copies you will still have brown eyes).</div><div><br></div>]]></description>
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         <pubDate>2017-08-09 05:34:47 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451545</guid>
      </item>
      <item>
         <title>Nonsense Mutations</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451613</link>
         <description><![CDATA[<div>Detrimental mutations truncate the gene sequence (<em>nonsense mutations</em>) to abrogate the normal function of a trait<br><br>All creds to BioNinja</div><div><br></div><div><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:36:48 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451613</guid>
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      <item>
         <title>Genome</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451655</link>
         <description><![CDATA[<div>The genome is the totality of genetic information of a cell, organism or organelle<br><br></div><div>All creds to BioNinja</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:38:05 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451655</guid>
      </item>
      <item>
         <title>Insertion mutations</title>
         <author>shania_sharma</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451679</link>
         <description><![CDATA[<div>(We think)&nbsp;<br><br>The addition of a different nucleotide base pair into the natural genetic sequence to produce a mutation.&nbsp;</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:38:36 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451679</guid>
      </item>
      <item>
         <title>Frame shift mutation</title>
         <author>arunima_shrikhande</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451685</link>
         <description><![CDATA[<div>A mutation caused by the addition or the deletion of a base pair or pairs, in the DNA sequence of a gene. It causes an unnatural reading frame of the DNA, from the mutation to the end of the gene.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:38:43 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451685</guid>
      </item>
      <item>
         <title>Missense mutation</title>
         <author>nandan_venkatesan</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451690</link>
         <description><![CDATA[<div>a <strong>missense mutation</strong> is a point <strong>mutation</strong>in which a single nucleotide change results in a codon that codes for a different amino acid.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:38:51 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451690</guid>
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      <item>
         <title>Locus</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451755</link>
         <description><![CDATA[<div>A <strong><em>locus</em></strong> is a spot or “address” on a chromosome at which a <strong><em>gene</em></strong> for a particular trait is located in all members of a species. It can also refer to the location of a mutation or other <strong><em>genetic</em></strong> marker. A given<strong><em>locus</em></strong> can be found on any pair of homologous chromosomes </div>]]></description>
         <enclosure url="https://www.youtube.com/watch?v=A_nVpHPSxpQ" />
         <pubDate>2017-08-09 05:39:45 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451755</guid>
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      <item>
         <title></title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451776</link>
         <description><![CDATA[]]></description>
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         <pubDate>2017-08-09 05:39:57 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451776</guid>
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      <item>
         <title>Mutations</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451851</link>
         <description><![CDATA[<div>A change in an organism's genetic code</div><div><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:41:07 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451851</guid>
      </item>
      <item>
         <title>Deletion Mutations</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451857</link>
         <description><![CDATA[<div>A deletion mutation occurs when part of a DNA molecule is not copied during DNA replication. This uncopied part can be as small as a single nucleotide or as much as an entire chromosome. The loss of this DNA during replication can lead to a genetic disease.</div>]]></description>
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         <pubDate>2017-08-09 05:41:09 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451857</guid>
      </item>
      <item>
         <title>Allele Frequency</title>
         <author></author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451933</link>
         <description><![CDATA[<div>the proportion of an allele within a population</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 05:42:16 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451933</guid>
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      <item>
         <title></title>
         <author>arunima_shrikhande</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180451938</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://ghr.nlm.nih.gov/primer/illustrations/frameshift.jpg" />
         <pubDate>2017-08-09 05:42:19 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180451938</guid>
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         <title>Genotype (2)</title>
         <author>arunima_shrikhande</author>
         <link>https://padlet.com/poonam_singhal/genetics/wish/180453784</link>
         <description><![CDATA[<div>Arrangement of the nucleotides in genomes, responsible for a certain physical trait or phenotype.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-08-09 06:10:27 UTC</pubDate>
         <guid>https://padlet.com/poonam_singhal/genetics/wish/180453784</guid>
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