Genomics England

ARL6

ADP ribosylation factor like GTPase 6

Panel	Mode of inheritance	Details
Filter panels11 panels
Green in Bardet Biedl syndrome R-numbers: R107 Signed-off version 2.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes ?Retinitis pigmentosa 55, 613575, {Bardet Biedl syndrome 1, modifier of}, 209900, Bardet Biedl syndrome 3, 600151
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 3.1	BIALLELIC, autosomal or pseudoautosomal	Phenotypes RETINITIS PIGMENTOSA TYPE 55 613575, BARDET-BIEDL SYNDROME TYPE 3 209900
Green in Fetal anomalies R-numbers: R21, R412 Signed-off version 3.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes BARDET-BIEDL SYNDROME TYPE 3, RETINITIS PIGMENTOSA TYPE 55
Green in Intellectual disability - microarray and sequencing Component of the following Super Panels: - Childhood onset leukodystrophy - Hypotonic infant - Paediatric disorders R-numbers: R29 Signed-off version 5.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Bardet-Biedl syndrome 3, 209900{Bardet-Biedl syndrome 1, modifier of}, 209900Retinitis pigmentosa 55, 613575, BARDET-BIEDL SYNDROME TYPE 3 (BBS3)
Green in Limb disorders Component of the following Super Panels: - Paediatric disorders Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Polydactyly, Bardet-Biedl syndrome 3 600151
Green in Ophthalmological ciliopathies Component of the following Super Panels: - Paediatric disorders - Rare multisystem ciliopathy Super panel Signed-off version 3.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes {Bardet Biedl syndrome 1, modifier of}, Bardet-Biedl Syndrome, 268000, Bardet Biedl syndrome 3
Green in Renal ciliopathies Component of the following Super Panels: - Cystic renal disease - Paediatric disorders - Rare multisystem ciliopathy Super panel Signed-off version 3.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes {Bardet Biedl syndrome 1, modifier of}, Bardet-Biedl Syndrome, 268000, Bardet Biedl syndrome 3
Green in Retinal disorders R-numbers: R32 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Eye Disorders, Bardet-Biedl syndrome 3, 209900, {Bardet-Biedl syndrome 1, modifier of}, 209900, Retinitis pigmentosa 55, 613575, Retinitis Pigmentosa, Recessive
Green in Severe early-onset obesity R-numbers: R149 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Obesity, Bardet-Biedl syndrome 3, OMIM:600151
Green in Skeletal dysplasia Component of the following Super Panels: - Paediatric disorders R-numbers: R104 Signed-off version 4.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Polydactyly, Bardet-Biedl syndrome 3 600151
Green in Unexplained young onset end-stage renal disease R-numbers: R257 Signed-off version 3.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Ciliopathy genes associated with cystic kidney disease, Bardel-Biedl syndrome type 3 600151