Previous symbols: WBSCR6. Aliases: TFII-I, BAP-135, SPIN, BTKAP1, DIWS, IB291.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Good Syndrome | unknown somatic |
mechanism: Thymic Epithelial Neoplasia
|
| Thymoma |
untyped
Recurrent somatic driver mutation
|
mechanism: GTF2I-driven thymic epithelial transformation; Impaired thymic epithelial progenitor differentiation; Metabolic stress survival program
|
| Williams Syndrome | untyped |
mechanism: GTF2I-Linked Myelination and Social-Behavior Circuit Dysfunction; Neurodevelopmental Interval-Gene Haploinsufficiency
animal model: Mus musculus
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.