DMXL2 Chromosome 15

Dmx like 2
68 variants 68 Health Risk

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What This Gene Does
This gene encodes a protein with 12 WD domains. Proteins with WD domains are involved in many functions including participation in signal transduction pathways. Participation of the encoded protein in regulation of the Notch signaling pathway has been demonstrated in vitro using several human cell lines (PMID:20810660). A gene encoding a similar protein is located on chromosome 5. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
Gene Info
Gene Group
WD repeat domain containing
Locus Type
gene with protein product
Location
15q21.2
Ensembl
ENSG00000104093
Associated Conditions (11)
Autism spectrum disorder
Inborn genetic diseases
DMXL2-related disorder
Developmental and epileptic encephalopathy
81
Polyendocrine-polyneuropathy syndrome
Hearing loss
autosomal dominant 71
Nonsyndromic genetic hearing loss
See cases
Acute myeloid leukemia
Key Variants
All Variants (68)
RSID Category Clinical Significance Conditions
RS1416564508 Health Risk association Autism spectrum disorder, Autism spectrum disorder
RS117017152 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS138394487 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, DMXL2-related disorder, Developmental and epileptic encephalopathy
RS139139263 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS143319761 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS143850714 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, DMXL2-related disorder, Inborn genetic diseases
RS145006217 Health Risk Conflicting classifications of pathogenicity Hearing loss, autosomal dominant 71, Hearing loss
RS148766950 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, DMXL2-related disorder, Nonsyndromic genetic hearing loss
RS149028181 Health Risk Conflicting classifications of pathogenicity Hearing loss, autosomal dominant 71, Hearing loss
RS149842282 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS182672196 Health Risk Conflicting classifications of pathogenicity
RS199806210 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2548745534 Health Risk Conflicting classifications of pathogenicity
RS367772050 Health Risk Conflicting classifications of pathogenicity Hearing loss, autosomal dominant 71, Hearing loss
RS372199887 Health Risk Conflicting classifications of pathogenicity
RS373506145 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375142338 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS376728796 Health Risk Conflicting classifications of pathogenicity Polyendocrine-polyneuropathy syndrome, Hearing loss, autosomal dominant 71
RS530791761 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Nonsyndromic genetic hearing loss, Inborn genetic diseases
RS606231461 Health Risk Conflicting classifications of pathogenicity Polyendocrine-polyneuropathy syndrome, See cases, Polyendocrine-polyneuropathy syndrome
RS746954557 Health Risk Conflicting classifications of pathogenicity
RS748480363 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS754786373 Health Risk Conflicting classifications of pathogenicity Hearing loss, autosomal dominant 71, Hearing loss
RS758539671 Health Risk Conflicting classifications of pathogenicity Acute myeloid leukemia, Acute myeloid leukemia
RS759451054 Health Risk Conflicting classifications of pathogenicity
RS768003104 Health Risk Conflicting classifications of pathogenicity
RS770629684 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS774515934 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, DMXL2-related disorder, Inborn genetic diseases
RS775660410 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778580507 Health Risk Conflicting classifications of pathogenicity Hearing loss, autosomal dominant 71, Hearing loss
RS2041613817 Health Risk Likely pathogenic
RS2140551864 Health Risk Likely pathogenic
RS2542973615 Health Risk Likely pathogenic
RS2542980248 Health Risk Likely pathogenic
RS2548417170 Health Risk Likely pathogenic
RS2548486231 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 81, Developmental and epileptic encephalopathy
RS2548703107 Health Risk Likely pathogenic
RS748413058 Health Risk Likely pathogenic
RS911230770 Health Risk Likely pathogenic
RS1192453905 Health Risk Pathogenic
RS1303032996 Health Risk Pathogenic
RS1372482877 Health Risk Pathogenic
RS1595908479 Health Risk Pathogenic Developmental and epileptic encephalopathy, 81, Developmental and epileptic encephalopathy
RS1595955503 Health Risk Pathogenic Developmental and epileptic encephalopathy, 81, Developmental and epileptic encephalopathy
RS1596016716 Health Risk Pathogenic Developmental and epileptic encephalopathy, 81, Developmental and epileptic encephalopathy
RS2042010887 Health Risk Pathogenic
RS2140933776 Health Risk Pathogenic Hearing loss, autosomal dominant 71, Hearing loss
RS2542973463 Health Risk Pathogenic
RS2543069732 Health Risk Pathogenic
RS2548416335 Health Risk Pathogenic
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