rs1057521927
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
|
28211990 |
2017 |
rs1057521927
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment.
|
28334956 |
2017 |
rs773618224
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
|
28211990 |
2017 |
rs773618224
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment.
|
28334956 |
2017 |
rs1057521927
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.
|
26539891 |
2015 |
rs773618224
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.
|
26539891 |
2015 |
rs1057521927
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1085308033
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs1085308033
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs752599948
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs752599948
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs767769359
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs767769359
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs773618224
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs200618384
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs886039608
|
Entrez Id: |
58497 |
Gene Symbol: |
PRUNE1 |
PRUNE1
|
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|