rs10896090
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Bipolar Disorder
A
0.700
GeneticVariation
GWASCAT
Genome-wide association study identifies 30 loci associated with bipolar disorder.
31043756
2019
rs187649293
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Finding of Mean Corpuscular Hemoglobin
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
T
0.810
CausalMutation
CLINVAR
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.
26795593
2016
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
0.810
GeneticVariation
UNIPROT
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.
23159249
2012
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
T
0.810
CausalMutation
CLINVAR
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.
23159249
2012
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
T
0.810
GeneticVariation
CLINVAR
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.
23159249
2012
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
0.810
GeneticVariation
BEFREE
Here we describe the first Indian patient with Schuurs-Hoeijmakers syndrome (SHMS ) with a de novo heterozygous NM_018026.3 (PACS1):c.607C>T (p.Arg203Trp ) variant.
30690871
2019
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Facial hemangioma
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Hydronephrosis
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Sacral dimple
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Muscle hypotonia
T
0.700
CausalMutation
CLINVAR
A novel missense mutation affecting the same amino acid as the recurrent PACS1 mutation in Schuurs-Hoeijmakers syndrome.
28975623
2018
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Small hand
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Dysmorphic features
T
0.700
CausalMutation
CLINVAR
Clinical delineation of the PACS1-related syndrome--Report on 19 patients.
26842493
2016
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Muscle hypotonia
T
0.700
CausalMutation
CLINVAR
Clinical delineation of the PACS1-related syndrome--Report on 19 patients.
26842493
2016
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Orbital separation diminished
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Smooth philtrum
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Muscle hypotonia
T
0.700
CausalMutation
CLINVAR
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.
23159249
2012
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Pallor of optic disc
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Multiple congenital anomalies
T
0.700
CausalMutation
CLINVAR
Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.
25356970
2015
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Muscle hypotonia
T
0.700
CausalMutation
CLINVAR
Association of the missense variant p.Arg203Trp in PACS1 as a cause of intellectual disability and seizures.
28111752
2017
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Dysmorphic features
T
0.700
CausalMutation
CLINVAR
A novel missense mutation affecting the same amino acid as the recurrent PACS1 mutation in Schuurs-Hoeijmakers syndrome.
28975623
2018
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Widely spaced teeth
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Aneurysm of aortic root
T
0.700
CausalMutation
CLINVAR
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Dysmorphic features
T
0.700
CausalMutation
CLINVAR
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.
23159249
2012
rs398123009
×
Entrez Id:
55690
Gene Symbol:
PACS1
PACS1
Mitral Valve Prolapse Syndrome
T
0.700
CausalMutation
CLINVAR