ST7 Chromosome 7
Suppression of tumorigenicity 7
Upload your DNA to see your personal genotypes for variants in ST7.
What This Gene Does
The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
MicroRNA protein coding host genes
Locus Type
gene with protein product
Location
7q31.2
Ensembl
ENSG00000004866
Associated Conditions (3)
Global developmental delay
Brain atrophy
Intractable seizure
Key Variants
All Variants (1)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS550492993 | Health Risk | Likely pathogenic | Global developmental delay, Brain atrophy, Intractable seizure |