BBS5

Bardet-Biedl syndrome 5
Identifiers
Symbol BBS5
External IDs OMIM: 603650 MGI: 1919819 HomoloGene: 12471 GeneCards: BBS5 Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 129880 72569
Ensembl ENSG00000163093 ENSMUSG00000063145
UniProt Q8N3I7 Q9CZQ9
RefSeq (mRNA) NM_152384 NM_028284
RefSeq (protein) NP_689597 NP_082560
Location (UCSC) Chr 2:
169.48 – 169.51 Mb
Chr 2:
69.65 – 69.67 Mb
PubMed search

Bardet-Biedl syndrome 5 protein is a protein that in humans is encoded by the BBS5 gene.[1][2][3]

This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized.[3]

External links

References

  1. Woods MO, Young TL, Parfrey PS, Hefferton D, Green JS, Davidson WS (Mar 1999). "Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus". Genomics 55 (1): 2–9. doi:10.1006/geno.1998.5626. PMID 9888993.
  2. Young TL, Penney L, Woods MO, Parfrey PS, Green JS, Hefferton D, Davidson WS (Apr 1999). "A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31". Am J Hum Genet 64 (3): 900–4. doi:10.1086/302301. PMC 1377810. PMID 10053027.
  3. 1 2 "Entrez Gene: BBS5 Bardet-Biedl syndrome 5".

Further reading

External links

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