This web page was produced as an assignment for Genetics 677 an undergraduate course at UW-Madison
BBS1-The Human Gene
The BBS1 gene encodes for a protein called BBS1. This gene, when mutated, causes Bardet-Biedl Syndrome. BBS1 is the most common gene that when mutated causes Bardet-Biedl Syndrome. The general information about the gene is located below.
To learn more about the protein click the button to the right. |
General Information [1]
Chromosome: 11
Cytogenetic Location: 11q13
Gene Length: 29,966 base pairs
Starts at base pair 66,278,118 ends on 66,301,083
Accession Number: NG_009093
FASTA
Cytogenetic Location: 11q13
Gene Length: 29,966 base pairs
Starts at base pair 66,278,118 ends on 66,301,083
Accession Number: NG_009093
FASTA
The Mutation M390R
To learn more about the WD40 domain found in BBS1, click the button on the right
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References:
[Banner Photo] "NDM-1" NDM-1. Retrieved 12 March 2013 from http://www.personal.psu.edu/czc5161/blogs/testing/references.html.
[1] "BBS1 Bardet-Biedl syndrome 1 [ Homo sapiens (human) ]." NCBI Gene. Retrieved 8 Feb 2013 from http://www.ncbi.nlm.nih.gov/gene/582.
[Banner Photo] "NDM-1" NDM-1. Retrieved 12 March 2013 from http://www.personal.psu.edu/czc5161/blogs/testing/references.html.
[1] "BBS1 Bardet-Biedl syndrome 1 [ Homo sapiens (human) ]." NCBI Gene. Retrieved 8 Feb 2013 from http://www.ncbi.nlm.nih.gov/gene/582.