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Gene: SLCO1B3

Red List (low evidence)

SLCO1B3 (solute carrier organic anion transporter family member 1B3)
EnsemblGeneIds (GRCh38): ENSG00000111700
EnsemblGeneIds (GRCh37): ENSG00000111700
OMIM: 605495, Gene2Phenotype
SLCO1B3 is in 3 panels

1 review

Louise Daugherty (Genomics England Curator)

I don't know

Each gene in the SFARI Human Gene module has a dedicated entry summary page, see here for more info on this gene:
Created: 1 Apr 2019, 11:26 a.m.


Clinvar variants
Variants in SLCO1B3
Panels with this gene

History Filter Activity

29 Mar 2019, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source Expert Review Red was added to SLCO1B3.

29 Mar 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: SLCO1B3 was added gene: SLCO1B3 was added to Autism. Sources: SFARI Mode of inheritance for gene: SLCO1B3 was set to