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Database ID
RNA ID
RNA Type
Disease Type
Disease Category
Sample Source
GEO ID
Detail
exR0082126
SPRY4
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082127
SPRYD3
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082128
SPRYD4
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082129
SPRYD7
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082130
SPSB1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082131
SPSB2
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082132
SPSB3
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082133
SPSB4
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082134
SPTA1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082135
SPTAN1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082136
SPTB
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082137
SPTBN1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082138
SPTBN2
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082139
SPTBN5
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail
exR0082140
SPTLC1
mRNA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Fragile X Syndrome
Amniotic Fluid Supernatant
GSE83556
Detail

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