SPEN Chromosome 1

Spen family transcriptional repressor
83 variants 83 Health Risk

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What This Gene Does
This gene encodes a hormone inducible transcriptional repressor. Repression of transcription by this gene product can occur through interactions with other repressors, by the recruitment of proteins involved in histone deacetylation, or through sequestration of transcriptional activators. The product of this gene contains a carboxy-terminal domain that permits binding to other corepressor proteins. This domain also permits interaction with members of the NuRD complex, a nucleosome remodeling protein complex that contains deacetylase activity. In addition, this repressor contains several RNA recognition motifs that confer binding to a steroid receptor RNA coactivator; this binding can modulate the activity of both liganded and nonliganded steroid receptors. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
RNA binding motif containing
Locus Type
gene with protein product
Location
1p36.21-p36.13
Ensembl
ENSG00000065526
Associated Conditions (10)
Developmental disorder
Radio-Tartaglia syndrome
Inborn genetic diseases
SPEN-related disorder
See cases
Neurodevelopmental delay
Myoepithelial tumor
Neurodevelopmental abnormality
Autism spectrum disorder
Encephalopathy
Key Variants
All Variants (83)
RSID Category Clinical Significance Conditions
RS1460194680 Health Risk Conflicting classifications of pathogenicity Developmental disorder, Radio-Tartaglia syndrome, Developmental disorder
RS148348676 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS149173601 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS150756182 Health Risk Conflicting classifications of pathogenicity SPEN-related disorder, SPEN-related disorder
RS199982380 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2071226510 Health Risk Conflicting classifications of pathogenicity Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2148737840 Health Risk Conflicting classifications of pathogenicity Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2148741011 Health Risk Conflicting classifications of pathogenicity Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS368139168 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS745655301 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS751475729 Health Risk Conflicting classifications of pathogenicity Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS752974887 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS754293393 Health Risk Conflicting classifications of pathogenicity
RS760431541 Health Risk Conflicting classifications of pathogenicity See cases, Inborn genetic diseases, See cases
RS764445929 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS767932162 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1399970491 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2070991188 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2148738318 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2148739946 Health Risk Likely pathogenic Neurodevelopmental delay, Neurodevelopmental delay
RS2148740737 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2148742017 Health Risk Likely pathogenic
RS2522936339 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2523072296 Health Risk Likely pathogenic SPEN-related disorder, SPEN-related disorder
RS2523072429 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2523072505 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2523073518 Health Risk Likely pathogenic
RS2523075382 Health Risk Likely pathogenic SPEN-related disorder, SPEN-related disorder
RS2523080343 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2523089310 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2523095875 Health Risk Likely pathogenic SPEN-related disorder, SPEN-related disorder
RS2523096849 Health Risk Likely pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS1386910185 Health Risk Pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS1458311779 Health Risk Pathogenic
RS1557761571 Health Risk Pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2071187754 Health Risk Pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2071203144 Health Risk Pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2071205857 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2071207771 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2071236139 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2071239657 Health Risk Pathogenic Inborn genetic diseases, Radio-Tartaglia syndrome, Inborn genetic diseases
RS2148733237 Health Risk Pathogenic
RS2148737783 Health Risk Pathogenic
RS2148737960 Health Risk Pathogenic
RS2148738489 Health Risk Pathogenic
RS2148738538 Health Risk Pathogenic
RS2148738629 Health Risk Pathogenic
RS2148739431 Health Risk Pathogenic Radio-Tartaglia syndrome, Radio-Tartaglia syndrome
RS2148740239 Health Risk Pathogenic
RS2148740780 Health Risk Pathogenic Neurodevelopmental delay, Neurodevelopmental delay
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