aggressive behavior Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Aggressive behavior can denote verbal aggression, physical aggression against objects, physical aggression against people, and may also include aggression towards oneself. (Human Phenotype Ontology, HP_0000718)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000718
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Genes

72 genes associated with the aggressive behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADSL adenylosuccinate lyase
AFF2 AF4/FMR2 family, member 2
ALDH5A1 aldehyde dehydrogenase 5 family, member A1
AMT aminomethyltransferase
ANK3 ankyrin 3, node of Ranvier (ankyrin G)
ATP13A2 ATPase type 13A2
CASC5 cancer susceptibility candidate 5
CEP152 centrosomal protein 152kDa
CHMP2B charged multivesicular body protein 2B
DEAF1 DEAF1 transcription factor
DHCR7 7-dehydrocholesterol reductase
DPAGT1 dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)
ECM1 extracellular matrix protein 1
EHMT1 euchromatic histone-lysine N-methyltransferase 1
FIG4 FIG4 phosphoinositide 5-phosphatase
FOXP1 forkhead box P1
GCSH glycine cleavage system protein H (aminomethyl carrier)
GLDC glycine dehydrogenase (decarboxylating)
GRIA3 glutamate receptor, ionotropic, AMPA 3
HDAC4 histone deacetylase 4
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
HSD17B10 hydroxysteroid (17-beta) dehydrogenase 10
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
KCNT1 potassium channel, sodium activated subfamily T, member 1
KDM5C lysine (K)-specific demethylase 5C
KMT2A lysine (K)-specific methyltransferase 2A
LEPR leptin receptor
LINS lines homolog (Drosophila)
MAN1B1 mannosidase, alpha, class 1B, member 1
MANBA mannosidase, beta A, lysosomal
MAOA monoamine oxidase A
MBD5 methyl-CpG binding domain protein 5
MED12 mediator complex subunit 12
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NAGLU N-acetylglucosaminidase, alpha
NAGS N-acetylglutamate synthase
NDP Norrie disease (pseudoglioma)
NSDHL NAD(P) dependent steroid dehydrogenase-like
OCRL oculocerebrorenal syndrome of Lowe
PAH phenylalanine hydroxylase
PAK3 p21 protein (Cdc42/Rac)-activated kinase 3
PCDH19 protocadherin 19
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PRNP prion protein
PRODH proline dehydrogenase (oxidase) 1
RBBP8 retinoblastoma binding protein 8
SATB2 SATB homeobox 2
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8
SLITRK1 SLIT and NTRK-like family, member 1
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SPAST spastin
SPR sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)
SYN1 synapsin I
TBP TATA box binding protein
TBX1 T-box 1
TCF4 transcription factor 4
TMEM231 transmembrane protein 231
TREM2 triggering receptor expressed on myeloid cells 2
TTC19 tetratricopeptide repeat domain 19
TTI2 TELO2 interacting protein 2
TYROBP TYRO protein tyrosine kinase binding protein
UBE2A ubiquitin-conjugating enzyme E2A
UQCC2 ubiquinol-cytochrome c reductase complex assembly factor 2
UROC1 urocanate hydratase 1
USP9X ubiquitin specific peptidase 9, X-linked
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)
WDR45 WD repeat domain 45
WDR62 WD repeat domain 62
ZBTB20 zinc finger and BTB domain containing 20