SCLT1
HGNC:26406 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in SCLT1 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| congenital heart disease | — | 1 | 1 |
Linked variants
Variants normalized to SCLT1| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|
No structured population context is available.
Supporting publications
2 records- 2019Autozygome and high throughput confirmation of disease genes candidacy.Genetics in medicine : official journal of the American College of Medical GeneticsPubMed ↗
- 2014Ciliary genes TBC1D32/C6orf170 and SCLT1 are mutated in patients with OFD type IX.Human mutationPubMed ↗