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Ciliopathies v0.174 BBIP1 Zornitza Stark edited their review of gene: BBIP1: Changed publications: 24026985, 32055034
Ciliopathies v0.174 BBIP1 Zornitza Stark Publications for gene: BBIP1 were set to 24026985
Ciliopathies v0.162 BBIP1 Elena Savva edited their review of gene: BBIP1: Added comment: PMID: 24026985 - Single patient with BBS described with bi-allelic variants in this gene.

PMID: 32055034 - An additional patient with classic BBS with a homozygous splice variant confirmed by RT-PCR to result in NMD

Only one other 'pathogenic' variant in ClinVar but homozygous missense and no evidence provided.; Changed phenotypes: Bardet-Biedl Syndrome
Ciliopathies v0.162 BBIP1 Elena Savva reviewed gene: BBIP1: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 24026985; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ciliopathies v0.56 BBIP1 Zornitza Stark Marked gene: BBIP1 as ready
Ciliopathies v0.56 BBIP1 Zornitza Stark Gene: bbip1 has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.56 BBIP1 Zornitza Stark Classified gene: BBIP1 as Amber List (moderate evidence)
Ciliopathies v0.56 BBIP1 Zornitza Stark Gene: bbip1 has been classified as Amber List (Moderate Evidence).
Ciliopathies v0.55 BBIP1 Zornitza Stark gene: BBIP1 was added
gene: BBIP1 was added to Ciliopathies_VCGS. Sources: Expert list
Mode of inheritance for gene: BBIP1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: BBIP1 were set to 24026985
Phenotypes for gene: BBIP1 were set to Bardet-Biedl syndrome 18, MIM#615995
Review for gene: BBIP1 was set to AMBER
Added comment: Single patient described with bi-allelic variants in this gene. Only one other 'pathogenic' variant in ClinVar but homozygous missense and no evidence provided.
Sources: Expert list