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| Heterotaxy v1.10 | TTC21B | Zornitza Stark Marked gene: TTC21B as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Heterotaxy v1.10 | TTC21B | Zornitza Stark Gene: ttc21b has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Heterotaxy v1.10 | TTC21B |
Zornitza Stark gene: TTC21B was added gene: TTC21B was added to Heterotaxy. Sources: Literature Mode of inheritance for gene: TTC21B was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TTC21B were set to 33547761 Phenotypes for gene: TTC21B were set to Heterotaxy Review for gene: TTC21B was set to RED Added comment: Bi-allelic variants in this gene are associated with a range of ciliopathies. Single family reported with two sibs, heterotaxy, and bi-allelic variants in this gene. One sib has additional ciliopathy features. Sources: Literature |
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