Gene Gene information from NCBI Gene database.
Entrez ID 129880
Gene name Bardet-Biedl syndrome 5
Gene symbol BBS5
Synonyms (NCBI Gene)
-
Chromosome 2
Chromosome location 2q31.1
Summary 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 eukaryot
SNPs SNP information provided by dbSNP.
22
SNP ID Visualize variation Clinical significance Consequence
rs121908581 G>A Pathogenic Coding sequence variant, missense variant
rs121908582 A>G Pathogenic Coding sequence variant, missense variant
rs137853921 A>G Conflicting-interpretations-of-pathogenicity, likely-pathogenic Coding sequence variant, missense variant
rs143191074 A>G Benign, conflicting-interpretations-of-pathogenicity Coding sequence variant, missense variant
rs179363897 G>A Pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
546
miRTarBase ID miRNA Experiments Reference
MIRT631876 hsa-miR-508-5p HITS-CLIP 23824327
MIRT664456 hsa-miR-1273g-3p HITS-CLIP 23824327
MIRT631875 hsa-miR-6849-3p HITS-CLIP 23824327
MIRT631874 hsa-miR-939-3p HITS-CLIP 23824327
MIRT631873 hsa-miR-766-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
32
GO ID Ontology Definition Evidence Reference
GO:0001947 Process Heart looping ISS
GO:0005515 Function Protein binding IPI 16327777, 17574030, 18762586, 20080638, 22500027, 24550735, 24939912, 25416956, 25552655, 27173435, 29039417, 33144677, 33961781
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol TAS
GO:0005856 Component Cytoskeleton IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603650 970 ENSG00000163093
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N3I7
Protein name BBSome complex member BBS5 (Bardet-Biedl syndrome 5 protein)
Protein function The BBSome complex is thought to function as a coat complex required for sorting of specific membrane proteins to the primary cilia. The BBSome complex is required for ciliogenesis but is dispensable for centriolar satellite function. This cilio
PDB 6XTB
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07289 BBL5 7 339 Bardet-Biedl syndrome 5 protein Family
Sequence
Sequence length 341
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    BBSome-mediated cargo-targeting to cilium
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
514
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Bardet-Biedl syndrome Pathogenic; Likely pathogenic rs1471916487, rs2105291750, rs373396081, rs1574339529, rs2105297751, rs2105300418, rs2105304338, rs2105297825, rs1172161975, rs2468033187, rs756684256, rs786205636, rs1285925896, rs759233586, rs2105290053
View all (26 more)
RCV002546737
RCV001378765
RCV001383653
RCV001866093
RCV001925601
RCV001893329
RCV002049554
RCV001941617
RCV005095820
RCV002470156
RCV003073272
RCV000256439
RCV002633055
RCV002760635
RCV002866363
RCV002307356
RCV003633480
RCV000787535
RCV003150848
RCV003222518
RCV003224781
RCV003524867
RCV003523702
RCV003633959
RCV003633119
RCV003633189
RCV003633319
RCV003633298
RCV003876021
RCV003882678
RCV000638356
RCV003633534
RCV005091977
RCV000690428
RCV000707557
RCV000735933
RCV000735934
RCV000058870
RCV005093027
RCV001059256
RCV001059630
RCV001229656
Bardet-Biedl syndrome 5 Pathogenic; Likely pathogenic rs1471916487, rs373396081, rs1683644409, rs1574339529, rs2105303591, rs536117380, rs1172161975, rs786205636, rs1285925896, rs2468033258, rs587777828, rs767221160, rs121908581, rs121908582, rs2468041599
View all (15 more)
RCV001335471
RCV005023140
RCV001526710
RCV001780411
RCV001808003
RCV002227838
RCV002249291
RCV003984827
RCV005028280
RCV002510680
RCV000006532
RCV000006533
RCV000006535
RCV000006536
RCV000006537
RCV003448659
RCV005030207
RCV005030216
RCV003988160
RCV005030355
RCV000502319
RCV001250528
RCV000678526
RCV000678527
RCV000763466
RCV005027880
RCV005027889
RCV000785901
RCV005025111
RCV001002712
RCV005029641
RCV002491729
BBS5-related disorder Pathogenic; Likely pathogenic rs2105300418, rs1238632042, rs1054138918, rs1272140892 RCV004753416
RCV003403181
RCV003392526
RCV004753002
Cone dystrophy Likely pathogenic rs1238632042 RCV000504629
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs16856986 RCV005924383
Bardet-Biedl syndrome 1 Uncertain significance; Conflicting classifications of pathogenicity rs763696357, rs753234582 RCV003229079
RCV003229005
Cervical cancer Conflicting classifications of pathogenicity rs143191074 RCV005887675
Cholangiocarcinoma Conflicting classifications of pathogenicity rs137853921 RCV005887782
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Bardet Biedl Syndrome Associate 10577922, 11179009, 12677556, 16723438, 26325687, 27708425, 29806606, 30850397, 31760295, 37239474, 37240074, 37293956
Deafness Autosomal Recessive 31 Associate 29806606
Diabetic Retinopathy Associate 23562823
Genetic Diseases Inborn Stimulate 16723438
Inflammation Associate 23562823
Muscular Dystrophy Congenital Megaconial Type Associate 37240074