FOXP1 Chromosome 3

Forkhead box P1
184 variants 184 Health Risk

Upload your DNA to see your personal genotypes for variants in FOXP1.

What This Gene Does
This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Forkhead box P1 protein contains both DNA-binding- and protein-protein binding-domains. This gene may act as a tumor suppressor as it is lost in several tumor types and maps to a chromosomal region (3p14.1) reported to contain a tumor suppressor gene(s). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Forkhead boxes|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
3p13
Ensembl
ENSG00000114861
Associated Conditions (25)
Intellectual disability
Anterior creases of earlobe
Delayed speech and language development
Strabismus
Glabellar hemangioma
Intellectual disability-severe speech delay-mild dysmorphism syndrome
Inborn genetic diseases
FOXP1-related disorder
Autism spectrum disorder
Familial cancer of breast
Cerebellar vermis hypoplasia
Congenital cerebellar hypoplasia
Autism
Squamous cell lung carcinoma
Melanoma
Neurodevelopmental disorder
See cases
Acute myeloid leukemia
INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
Seizure
+5 more conditions
Key Variants
All Variants (184)
RSID Category Clinical Significance Conditions
RS969304991 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS987536405 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1057518999 Health Risk Likely pathogenic Autism, Autism
RS1064795306 Health Risk Likely pathogenic
RS1234028937 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS1553656383 Health Risk Likely pathogenic
RS1553660900 Health Risk Likely pathogenic
RS1559596230 Health Risk Likely pathogenic
RS1559596699 Health Risk Likely pathogenic
RS1559617016 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS1559621862 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Squamous cell lung carcinoma, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS1575757812 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS1575806033 Health Risk Likely pathogenic
RS1576028676 Health Risk Likely pathogenic Intellectual disability, Intellectual disability
RS2037853932 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2040036225 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2040037008 Health Risk Likely pathogenic
RS2106869182 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2107113697 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2107155481 Health Risk Likely pathogenic Melanoma, Melanoma
RS2107157863 Health Risk Likely pathogenic
RS2107201851 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2107310071 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2107612940 Health Risk Likely pathogenic
RS2107613139 Health Risk Likely pathogenic Neurodevelopmental disorder, Neurodevelopmental disorder
RS2544931486 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545047340 Health Risk Likely pathogenic
RS2545050061 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545110016 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545110459 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545110718 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545110803 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, See cases, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545119133 Health Risk Likely pathogenic Acute myeloid leukemia, Acute myeloid leukemia
RS2545120168 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545265597 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545413144 Health Risk Likely pathogenic
RS2545543007 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545873713 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS2545885560 Health Risk Likely pathogenic
RS587777855 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS786200948 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS797045586 Health Risk Likely pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Inborn genetic diseases, Intellectual disability
RS1057524732 Health Risk Pathogenic
RS1064793944 Health Risk Pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS1064796914 Health Risk Pathogenic
RS112795301 Health Risk Pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS1135401796 Health Risk Pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome, Intellectual disability-severe speech delay-mild dysmorphism syndrome
RS1553656387 Health Risk Pathogenic
RS1553660890 Health Risk Pathogenic
RS1553667322 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
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