Gene: SCLT1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 132320
Gene Symbol: SCLT1
SCLT1 		0.310 Biomarker disease GENOMICS_ENGLAND Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome. 30425282 2018
Entrez Id: 132320
Gene Symbol: SCLT1
SCLT1 		0.310 GeneticVariation disease BEFREE Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome. 30425282 2018
Entrez Id: 132320
Gene Symbol: SCLT1
SCLT1 		0.310 Biomarker disease GENOMICS_ENGLAND Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing. 28005958 2016
Entrez Id: 132320
Gene Symbol: SCLT1
SCLT1 		0.310 Biomarker disease GENOMICS_ENGLAND Ciliary genes TBC1D32/C6orf170 and SCLT1 are mutated in patients with OFD type IX. 24285566 2014