Loci

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Full Dataset

TRGT definitions for genotyping in PacBio HiFi reads:
hg19 hg38 T2T-chm13

Extended BED format for filtering genomic data:
hg19 hg38 T2T-chm13

Table

Full table of tandem repeat loci associated with Mendelian diseases.

6 loci
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ARSBMASpinal and bulbar muscular atrophy, Kennedy DiseasechrX:67545316-67545419
GCA
XR
View
COMPEDM1, PSACHMultiple epiphyseal dysplasia, Pseudoachondroplasiachr19:18786034-18786050
GTC
AD
View
HOXD13SD5Syndactylychr2:176093058-176093103
GCN
AD
View
SOX3XLMRX-linked panhypopituitarism ; X-linked mental retardation with isolated growth hormonechrX:140504316-140504361
NGC
XR
View
VWA1HMNR7Neuronopathy, distal hereditary motor, autosomal recessive 7chr1:1435798-1435818
GGCGCGGAGC
AR
View
pre-MIR7-2CHNG3Nongoitrous congenital hypothyroidism-3chr15:88569433-88569452
TTTG
AD
6 rows

Plots

High-level, visual overview of loci.

Pathogenic Size Range

110100100010kFAME4SCA10FAME3SCA36FAME6GDPAGCANVASFTDALS1FAME2FRA7ANMESCA27BFRA2AFRA12AFRAXEFXS, FXTAS, POF1SCA31FAME1OPML1EPM1OPDM4OPDMJBSDM2FAME7RCPSOPDM1OPDM2DBQD2, BSSSCA8XDPNIIDSCA3, MJDFRDASCA37SCA12FECD3DM1SCA17DRPLASCA4SCAHDHDL2CJDSCA1SBMASCA7SCA2CCHSTOFHPE5HFG-IHFG-IIISD5XLMRSCA6PRTSCCDHFG-IIHSAN VIIIEIEE1BPESFAME8OPMDVACTERLXEDM1, PSACHCHNG3HMNR7ADTKD
Allele sizeBenignIntermediatePathogenicAllele size in base pairsDisease

Age of Onset

020406080FECD3CJDSCA36FAME6SCA27BFTDALS1OPMDCANVASSCA37ADTKDFAME7SCA6OPML1SCA4OPDM2HDL2FAME1XDPSCA10OPDMFAME3NIIDOPDM4FAME4SBMASCA31SCA12OPDM1FAME8SCA1EPM1FAME2SCASCA3, MJDEDM1, PSACHSCA17SCA2FRDAGDPAGFRA7AFRAXEFRA2AHDNMEEIEE1PRTSDRPLASCA7SCA8DM2FRA12ADM1FXS, FXTAS, POF1CCHSXLMRHMNR7
InheritanceADARXDXRAge of onset (years)Disease