Mercurial > repos > dlalgroup > simtext_app
diff examples/data/1b/clingen_data @ 0:34ed44f3f85c draft
"planemo upload for repository https://github.com/dlal-group/simtext commit fd3f5b7b0506fbc460f2a281f694cb57f1c90a3c-dirty"
| author | dlalgroup |
|---|---|
| date | Thu, 24 Sep 2020 02:17:05 +0000 |
| parents | |
| children |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/examples/data/1b/clingen_data Thu Sep 24 02:17:05 2020 +0000 @@ -0,0 +1,96 @@ +"ID_gene" "GROUPING_disorder" +"1" "CHD2" "complex neurodevelopmental disorder" +"2" "EEF1A2" "complex neurodevelopmental disorder" +"3" "GRIN1" "complex neurodevelopmental disorder" +"4" "GRIN2A" "complex neurodevelopmental disorder" +"5" "KCNB1" "complex neurodevelopmental disorder" +"6" "MEF2C" "complex neurodevelopmental disorder" +"7" "NRXN1" "complex neurodevelopmental disorder" +"8" "PURA" "complex neurodevelopmental disorder" +"9" "SCN2A" "complex neurodevelopmental disorder" +"10" "SCN8A" "complex neurodevelopmental disorder" +"11" "SHANK2" "complex neurodevelopmental disorder" +"12" "SYNGAP1" "complex neurodevelopmental disorder" +"13" "CC2D1A" "complex neurodevelopmental disorder" +"14" "HOXA1" "complex neurodevelopmental disorder" +"15" "IQSEC2" "complex neurodevelopmental disorder" +"16" "NLGN4X" "complex neurodevelopmental disorder" +"17" "SMC1A" "complex neurodevelopmental disorder" +"18" "UPF3B" "complex neurodevelopmental disorder" +"19" "WDR45" "complex neurodevelopmental disorder" +"20" "ACTA2" "familial thoracic aortic aneurysm and aortic dissection" +"21" "COL3A1" "familial thoracic aortic aneurysm and aortic dissection" +"22" "FBN1" "familial thoracic aortic aneurysm and aortic dissection" +"23" "LOX" "familial thoracic aortic aneurysm and aortic dissection" +"24" "MYH11" "familial thoracic aortic aneurysm and aortic dissection" +"25" "MYLK" "familial thoracic aortic aneurysm and aortic dissection" +"26" "PRKG1" "familial thoracic aortic aneurysm and aortic dissection" +"27" "SMAD3" "familial thoracic aortic aneurysm and aortic dissection" +"28" "TGFB2" "familial thoracic aortic aneurysm and aortic dissection" +"29" "TGFBR1" "familial thoracic aortic aneurysm and aortic dissection" +"30" "TGFBR2" "familial thoracic aortic aneurysm and aortic dissection" +"31" "ACTG1" "nonsyndromic genetic deafness" +"32" "COCH" "nonsyndromic genetic deafness" +"33" "EYA4" "nonsyndromic genetic deafness" +"34" "GRHL2" "nonsyndromic genetic deafness" +"35" "KCNQ4" "nonsyndromic genetic deafness" +"36" "MYH14" "nonsyndromic genetic deafness" +"37" "MYO6" "nonsyndromic genetic deafness" +"38" "MYO7A" "nonsyndromic genetic deafness" +"39" "POU4F3" "nonsyndromic genetic deafness" +"40" "SLC17A8" "nonsyndromic genetic deafness" +"41" "TECTA" "nonsyndromic genetic deafness" +"42" "TMC1" "nonsyndromic genetic deafness" +"43" "CABP2" "nonsyndromic genetic deafness" +"44" "CDH23" "nonsyndromic genetic deafness" +"45" "CIB2" "nonsyndromic genetic deafness" +"46" "CLDN14" "nonsyndromic genetic deafness" +"47" "ESPN" "nonsyndromic genetic deafness" +"48" "ESRRB" "nonsyndromic genetic deafness" +"49" "GIPC3" "nonsyndromic genetic deafness" +"50" "GRXCR1" "nonsyndromic genetic deafness" +"51" "ILDR1" "nonsyndromic genetic deafness" +"52" "LHFPL5" "nonsyndromic genetic deafness" +"53" "LOXHD1" "nonsyndromic genetic deafness" +"54" "MARVELD2" "nonsyndromic genetic deafness" +"55" "MYO15A" "nonsyndromic genetic deafness" +"56" "MYO3A" "nonsyndromic genetic deafness" +"57" "OTOA" "nonsyndromic genetic deafness" +"58" "OTOG" "nonsyndromic genetic deafness" +"59" "OTOGL" "nonsyndromic genetic deafness" +"60" "PJVK" "nonsyndromic genetic deafness" +"61" "RDX" "nonsyndromic genetic deafness" +"62" "S1PR2" "nonsyndromic genetic deafness" +"63" "STRC" "nonsyndromic genetic deafness" +"64" "TMIE" "nonsyndromic genetic deafness" +"65" "TMPRSS3" "nonsyndromic genetic deafness" +"66" "TPRN" "nonsyndromic genetic deafness" +"67" "POU3F4" "nonsyndromic genetic deafness" +"68" "SMPX" "nonsyndromic genetic deafness" +"69" "KRAS" "Noonan syndrome" +"70" "LZTR1" "Noonan syndrome" +"71" "NRAS" "Noonan syndrome" +"72" "PTPN11" "Noonan syndrome" +"73" "RAF1" "Noonan syndrome" +"74" "RIT1" "Noonan syndrome" +"75" "RRAS2" "Noonan syndrome" +"76" "SOS1" "Noonan syndrome" +"77" "ETHE1" "Leigh syndrome" +"78" "LRPPRC" "Leigh syndrome" +"79" "NDUFS1" "Leigh syndrome" +"80" "NDUFS4" "Leigh syndrome" +"81" "NDUFV1" "Leigh syndrome" +"82" "SCO2" "Leigh syndrome" +"83" "SLC19A3" "Leigh syndrome" +"84" "SUCLA2" "Leigh syndrome" +"85" "SURF1" "Leigh syndrome" +"86" "TTC19" "Leigh syndrome" +"87" "PDHA1" "Leigh syndrome" +"88" "ACTC1" "hypertrophic cardiomyopathy" +"89" "MYH7" "hypertrophic cardiomyopathy" +"90" "MYL3" "hypertrophic cardiomyopathy" +"91" "PRKAG2" "hypertrophic cardiomyopathy" +"92" "TNNI3" "hypertrophic cardiomyopathy" +"93" "TNNT2" "hypertrophic cardiomyopathy" +"94" "TPM1" "hypertrophic cardiomyopathy" +"95" "ALPK3" "hypertrophic cardiomyopathy"