mental disorders Gene Set
| Dataset |
GAD Gene-Disease Associations
|
| Category |
disease or phenotype associations
|
| Type |
disease |
| Similar Terms |
|
| Downloads & Tools |
|
Genes
25 genes associated with the disease mental disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABCD1
|
ATP-binding cassette, sub-family D (ALD), member 1
|
|
ADAM19
|
ADAM metallopeptidase domain 19
|
|
ATP6V1B2
|
ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2
|
|
BPI
|
bactericidal/permeability-increasing protein
|
|
CNTNAP2
|
contactin associated protein-like 2
|
|
COL4A1
|
collagen, type IV, alpha 1
|
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COL4A2
|
collagen, type IV, alpha 2
|
|
EFNA5
|
ephrin-A5
|
|
ERC2
|
ELKS/RAB6-interacting/CAST family member 2
|
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FAM69A
|
family with sequence similarity 69, member A
|
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KMT2C
|
lysine (K)-specific methyltransferase 2C
|
|
MAD1L1
|
MAD1 mitotic arrest deficient-like 1 (yeast)
|
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MYO18B
|
myosin XVIIIB
|
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NALCN
|
sodium leak channel, non selective
|
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NCKAP5
|
NCK-associated protein 5
|
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NPAS3
|
neuronal PAS domain protein 3
|
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NTM
|
neurotrimin
|
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PAQR5
|
progestin and adipoQ receptor family member V
|
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PGPEP1
|
pyroglutamyl-peptidase I
|
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PHF8
|
PHD finger protein 8
|
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PTPRN2
|
protein tyrosine phosphatase, receptor type, N polypeptide 2
|
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RFX2
|
regulatory factor X, 2 (influences HLA class II expression)
|
|
SAA2
|
serum amyloid A2
|
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SMARCAD1
|
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
|
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VAT1L
|
vesicle amine transport 1-like
|
