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Table 2 Microsatellite markers employed in Mapping of chromosome 19 candidate region in consanguineous family (MPS001)

From: Germline mutations in RYR1 are associated with foetal akinesia deformation sequence/lethal multiple pterygium syndrome

Marker

Genomic position

Source

D19S222

Chr.19-28,725,890-28,726,217 bp

http://rgd.mcw.edu/rgdweb/report/marker/main.html?id=1341900

D19S433

Doesn’t map to Chr.19 assembly

http://rgd.mcw.edu/rgdweb/report/marker/main.html?id=1298168

D19S430

Chr.19-32,302,451-32,302,741 bp

http://rgd.mcw.edu/rgdweb/report/marker/main.html?id=1657125

D19S224

Chr.19-35,493,932-35,494,196 bp

http://rgd.mcw.edu/rgdweb/report/marker/main.html?id=1336138

Chr19r2-15xAC41

Chr.19-41,435,658-43,123,394

ftp://ftp.broad.mit.edu/pub/human_STS_releases/

D19S220

cHR.19-34,8798,595-34,879,871 BP

http://rgd.mcw.edu/rgdweb/search/markers.html?term=D19S220&speciesType=1

D19S228

Chr.19-34,937,645-34,937,798 bp

http://rgd.mcw.edu/rgdweb/report/marker/main.html?id=1338234

D19S421

Chr.19-38,871,106-38,871,460 bp

http://rgd.mcw.edu/rgdweb/report/marker/main.html?id=1337182

Chr19R2-15xTAT

Chr.19-44,221,282-44,669,155

ftp://ftp.broad.mit.edu/pub/human_STS_releases/

Chr19r2-22xGT44

Chr.19-44,221,282-44,669,155

ftp://ftp.broad.mit.edu/pub/human_STS_releases/