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BBS1 gene: MedlinePlus Genetics
medlineplus.gov
The BBS1 gene provides instructions for making a protein found in cells throughout the body. The BBS1 protein is part of a group (complex) of proteins that ...
BBS1 Gene - GeneCards | BBS1 Protein | BBS1 Antibody
www.genecards.org
Complete information for BBS1 gene (Protein Coding), Bardet-Biedl Syndrome 1, including: function, proteins, disorders, pathways, orthologs, and expression.
BBS1 - Bardet-Biedl syndrome 1 protein - Homo sapiens (Human ...
www.uniprot.org
The BBSome complex is thought to function as a coat complex required for sorting of specific membrane proteins to the primary cilia.
582 - Gene ResultBBS1 Bardet-Biedl syndrome 1 [ (human)]
www.ncbi.nlm.nih.gov
BBS1 Bardet-Biedl syndrome 1 [ (human)]. Gene ID: 582, updated on 5-Aug-2022. Summary. Mutations in this gene have been observed in patients with the major ...
Board of Behavioral Sciences (BBS)
www.bbs.ca.gov
In addition, on or after January 1, 2017, applicants for subsequent ASW, IMF, or PCCI registration must pass the California Law and Ethics Exam, before a ...
Entry - *209901 - BBS1 GENE; BBS1 - OMIM
www.omim.org
BBS1 is 1 of 7 BBS proteins that form the stable core of a protein complex required for ciliogenesis (Nachury et al., 2007).
BBS1 - Wikipedia
en.wikipedia.org
Bardet–Biedl syndrome 1 protein is a protein that in humans is encoded by the BBS1 gene. BBS1 is part of the BBSome complex, which required for ciliogenesis ...
Entry - #209900 - BARDET-BIEDL SYNDROME 1; BBS1 - OMIM
www.omim.org
Digenic inheritance has also been reported; see MOLECULAR GENETICS. ▽ Description. Bardet-Biedl syndrome is an autosomal recessive and genetically ...
Bardet-Biedl syndrome, BBS1-related | Myriad Foresight® Carrier ...
myriad.com
Bardet-Biedl Syndrome (BBS), BBS1-Related is an inherited disease that affects many different parts of the body. This condition generally causes vision ...
Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential ...
academic.oup.com
Abstract. Bardet–Biedl syndrome (BBS) is a pleiotropic genetic disorder with substantial inter- and intrafamilial variability, that also exhibits remarkable ...