SP9 Chromosome 2

Sp9 transcription factor
3 variants 3 Health Risk

Upload your DNA to see your personal genotypes for variants in SP9.

What This Gene Does
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Gene Info
Gene Group
"Zinc fingers C2H2-type|Sp transcription factors"
Locus Type
gene with protein product
Location
2q31.1
Ensembl
ENSG00000217236
Associated Conditions (8)
Abnormal caudate nucleus morphology
Epileptic encephalopathy
Intellectual disability
EEG abnormality
Hypotonia
SP9-associated disorder
Autistic behavior
6 conditions
Key Variants
All Variants (3)
RSID Category Clinical Significance Conditions
RS2105510219 Health Risk Pathogenic Abnormal caudate nucleus morphology, Epileptic encephalopathy, Intellectual disability
RS2105510265 Health Risk Pathogenic Autistic behavior, Intellectual disability, Autistic behavior
RS2105510286 Health Risk Pathogenic 6 conditions, 6 conditions
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