PAX3 Chromosome 2

Paired box 3
128 variants 128 Health Risk

Upload your DNA to see your personal genotypes for variants in PAX3.

What This Gene Does
This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t(2;13)(q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma. Alternative splicing results in transcripts encoding isoforms with different C-termini. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"PRD class homeoboxes and pseudogenes|Paired boxes"
Locus Type
gene with protein product
Location
2q36.1
Ensembl
ENSG00000135903
Associated Conditions (14)
Waardenburg syndrome type 1
Craniofacial-deafness-hand syndrome
Alveolar rhabdomyosarcoma
Waardenburg syndrome type 3
Waardenburg syndrome
Usher syndrome
PAX3-related disorder
Inborn genetic diseases
Hearing impairment
Congenital diaphragmatic hernia
Intellectual disability
Rare genetic deafness
Ocular albinism with congenital sensorineural hearing loss
See cases
Key Variants
RS1379006499
Conflicting classifications of pathogenicity
Waardenburg syndrome type 1, Waardenburg syndrome type 1
Health Risk
RS148454691
Conflicting classifications of pathogenicity
Craniofacial-deafness-hand syndrome, Alveolar rhabdomyosarcoma, Waardenburg syndrome type 1
Health Risk
RS151199924
Conflicting classifications of pathogenicity
Craniofacial-deafness-hand syndrome, Waardenburg syndrome, Usher syndrome
Health Risk
RS185119406
Conflicting classifications of pathogenicity
Waardenburg syndrome, Craniofacial-deafness-hand syndrome, Waardenburg syndrome
Health Risk
RS199560470
Conflicting classifications of pathogenicity
PAX3-related disorder, PAX3-related disorder
Health Risk
RS200679164
Conflicting classifications of pathogenicity
Craniofacial-deafness-hand syndrome, Waardenburg syndrome type 3, Alveolar rhabdomyosarcoma
Health Risk
RS200701839
Conflicting classifications of pathogenicity
Craniofacial-deafness-hand syndrome, Waardenburg syndrome, Hearing impairment
Health Risk
RS2234675
Conflicting classifications of pathogenicity
Congenital diaphragmatic hernia, Waardenburg syndrome, Craniofacial-deafness-hand syndrome
Health Risk
RS374429328
Conflicting classifications of pathogenicity
Waardenburg syndrome, Craniofacial-deafness-hand syndrome, Waardenburg syndrome
Health Risk
RS376147620
Conflicting classifications of pathogenicity
Waardenburg syndrome, Craniofacial-deafness-hand syndrome, Waardenburg syndrome
Health Risk
RS387906947
Conflicting classifications of pathogenicity
Waardenburg syndrome type 1, Waardenburg syndrome type 1, Waardenburg syndrome type 1
Health Risk
RS747502205
Conflicting classifications of pathogenicity
Waardenburg syndrome, Craniofacial-deafness-hand syndrome, Waardenburg syndrome
Health Risk
All Variants (128)
RSID Category Clinical Significance Conditions
RS1379006499 Health Risk Conflicting classifications of pathogenicity Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS148454691 Health Risk Conflicting classifications of pathogenicity Craniofacial-deafness-hand syndrome, Alveolar rhabdomyosarcoma, Waardenburg syndrome type 1
RS151199924 Health Risk Conflicting classifications of pathogenicity Craniofacial-deafness-hand syndrome, Waardenburg syndrome, Usher syndrome
RS185119406 Health Risk Conflicting classifications of pathogenicity Waardenburg syndrome, Craniofacial-deafness-hand syndrome, Waardenburg syndrome
RS199560470 Health Risk Conflicting classifications of pathogenicity PAX3-related disorder, PAX3-related disorder
RS200679164 Health Risk Conflicting classifications of pathogenicity Craniofacial-deafness-hand syndrome, Waardenburg syndrome type 3, Alveolar rhabdomyosarcoma
RS200701839 Health Risk Conflicting classifications of pathogenicity Craniofacial-deafness-hand syndrome, Waardenburg syndrome, Hearing impairment
RS2234675 Health Risk Conflicting classifications of pathogenicity Congenital diaphragmatic hernia, Waardenburg syndrome, Craniofacial-deafness-hand syndrome
RS374429328 Health Risk Conflicting classifications of pathogenicity Waardenburg syndrome, Craniofacial-deafness-hand syndrome, Waardenburg syndrome
RS376147620 Health Risk Conflicting classifications of pathogenicity Waardenburg syndrome, Craniofacial-deafness-hand syndrome, Waardenburg syndrome
RS387906947 Health Risk Conflicting classifications of pathogenicity Waardenburg syndrome type 1, Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS747502205 Health Risk Conflicting classifications of pathogenicity Waardenburg syndrome, Craniofacial-deafness-hand syndrome, Waardenburg syndrome
RS770424826 Health Risk Conflicting classifications of pathogenicity
RS776059693 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS104893652 Health Risk Likely pathogenic Craniofacial-deafness-hand syndrome, Craniofacial-deafness-hand syndrome
RS104893653 Health Risk Likely pathogenic Waardenburg syndrome type 3, Waardenburg syndrome type 3
RS1057524511 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1210072810 Health Risk Likely pathogenic
RS1279989885 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553568831 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553572740 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553572946 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553575157 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553575159 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553575179 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553575191 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553592703 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553592713 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553592757 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553592766 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553593874 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553593917 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553593928 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome, Waardenburg syndrome type 1
RS1553593965 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1553594554 Health Risk Likely pathogenic
RS1559320299 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1574771535 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1574772091 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1692619812 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1695251013 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS1695335992 Health Risk Likely pathogenic
RS200517998 Health Risk Likely pathogenic
RS2106074603 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS2106095025 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS2106203654 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS2106203794 Health Risk Likely pathogenic
RS2106203892 Health Risk Likely pathogenic Waardenburg syndrome type 1, Waardenburg syndrome type 1
RS2469196259 Health Risk Likely pathogenic PAX3-related disorder, PAX3-related disorder
RS2469197395 Health Risk Likely pathogenic
RS2469249189 Health Risk Likely pathogenic PAX3-related disorder, PAX3-related disorder
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