BBS12 (Bardet-Biedl syndrome 12)

2014-11-01  

Identity

HGNC
LOCATION
4q27
LOCUSID
ALIAS
C4orf24

Other Information

Locus ID:

NCBI: 166379
MIM: 610683
HGNC: 26648
Ensembl: ENSG00000181004

Variants:

dbSNP: 166379
ClinVar: 166379
TCGA: ENSG00000181004
COSMIC: BBS12

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000181004ENST00000314218Q6ZW61
ENSG00000181004ENST00000433287C9J8H7
ENSG00000181004ENST00000542236Q6ZW61

Expression (GTEx)

0
5
10
15

Pathways

PathwaySourceExternal ID
Organelle biogenesis and maintenanceREACTOMER-HSA-1852241
Cilium AssemblyREACTOMER-HSA-5617833
Cargo trafficking to the periciliary membraneREACTOMER-HSA-5620920
BBSome-mediated cargo-targeting to ciliumREACTOMER-HSA-5620922

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
372939562023Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variants.1
372939562023Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variants.1
246115922014Overview of Bardet-Biedl syndrome in Spain: identification of novel mutations in BBS1, BBS10 and BBS12 genes.12
246115922014Overview of Bardet-Biedl syndrome in Spain: identification of novel mutations in BBS1, BBS10 and BBS12 genes.12
229589202012BBS-induced ciliary defect enhances adipogenesis, causing paradoxical higher-insulin sensitivity, glucose usage, and decreased inflammatory response.47
229589202012BBS-induced ciliary defect enhances adipogenesis, causing paradoxical higher-insulin sensitivity, glucose usage, and decreased inflammatory response.47
204726602010Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population.35
208277842010Two sibs with Bardet-Biedl syndrome due to mutations in BBS12: no clues for modulation by a third mutation in BBS10.5
204726602010Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population.35
208277842010Two sibs with Bardet-Biedl syndrome due to mutations in BBS12: no clues for modulation by a third mutation in BBS10.5
191901842009Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation.92
191901842009Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation.92
171608892007Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome.93
171608892007Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome.93

Citation

Dessen P

BBS12 (Bardet-Biedl syndrome 12)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/60716/case-report-explorer/img/css/lib/bootstrap.min.css