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Human Gene Search Results


Unique ID Gene Symbol Gene Name Chromosome Loc Genetic Category Gene Ranking Biallelic # of Variants Associated Disorders # of Reports Primary Reference Display
GEN018 ASMT acetylserotonin O-methyltransferase Xp22.33 Rare Single Gene variant, Genetic Association
N
20 9 Melke J , et al. 2007 Edit
GEN173 NLGN4Y neuroligin 4, Y-linked Yq11.221 Genetic Association
N
0 3 Ylisaukko-oja T , et al. 2005 Edit
GEN821 SHOX short stature homeobox Yp11.2 Rare single gene variant
N
27 2 Tropeano M , et al. 2016 Edit
GEN313 USP9Y ubiquitin specific peptidase 9, Y-linked Yq11.221 Genetic Association
N
2 2 Wang K , et al. 2009 Edit

 

CNV Search Results


Chromosome
CNV Locus
CNV Type
# of studies
Animal Model
 
X
Deletion-Duplication
 33
 
 
X
Deletion
 1
 
 
X
Deletion
 3
 
 
X
Deletion-Duplication
 1
 
 
X
Deletion
 1
 
 
X
Duplication
 1
 
 
X
Duplication
 1
 
 
X
Deletion
 1
 
 
X
Deletion
 1
 
 
X
Duplication
 4
 
 
X
Deletion
 5
 
 
X
Duplication
 5
 
 
X
Deletion
 1
 
 
X
Deletion-Duplication
 12
 
 
X/Y
Duplication
 5
 
 
X/Y
Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Duplication
 2
 
 
Y
Deletion-Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Duplication
 5
 
 
Y
Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Duplication
 1
 
 
Y
Deletion
 1
 
 
Y
Duplication
 2
 
 
Y
Deletion
 2
 

 

Animal Model Search Results


Gene Symbol
Gene Name
Model Species
Syntenic
Primary Reference
Number of Reports
Number of Models

 

PIN Search Results


Gene Symbol
Gene Name
Number of Interactions
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