aggressive behavior Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A behavioral interaction between organisms in which one organism has the intention of inflicting physical damage on another individual. (Gene Ontology, GO_0002118)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000718
Similar Terms
Downloads & Tools

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