abnormal brain weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the average weight of the brain (Mammalian Phenotype Ontology, MP_0012775)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012775
Similar Terms
Downloads & Tools

Genes

72 gene mutations causing the abnormal brain weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADIPOR2 adiponectin receptor 2
AKT3 v-akt murine thymoma viral oncogene homolog 3
APP amyloid beta (A4) precursor protein
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
ASS1 argininosuccinate synthase 1
ATR ATR serine/threonine kinase
ATXN1 ataxin 1
B4GALT2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2
BCKDK branched chain ketoacid dehydrogenase kinase
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CAV1 caveolin 1, caveolae protein, 22kDa
CD81 CD81 molecule
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CENPJ centromere protein J
CERS1 ceramide synthase 1
CIT citron rho-interacting serine/threonine kinase
CTSF cathepsin F
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DDIT3 DNA-damage-inducible transcript 3
DEDD death effector domain containing
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
GHR growth hormone receptor
GNPAT glyceronephosphate O-acyltransferase
GPR85 G protein-coupled receptor 85
HAP1 huntingtin-associated protein 1
HDAC2 histone deacetylase 2
HSD17B2 hydroxysteroid (17-beta) dehydrogenase 2
HTRA2 HtrA serine peptidase 2
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
KIF14 kinesin family member 14
KLF3 Kruppel-like factor 3 (basic)
LAMA2 laminin, alpha 2
LPPR4 lipid phosphate phosphatase-related protein type 4
MBD1 methyl-CpG binding domain protein 1
MBD5 methyl-CpG binding domain protein 5
MECP2 methyl CpG binding protein 2
NBEA neurobeachin
NDE1 nudE neurodevelopment protein 1
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NPC1 Niemann-Pick disease, type C1
NRD1 nardilysin (N-arginine dibasic convertase)
OTX1 orthodenticle homeobox 1
PAPPA2 pappalysin 2
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
PFDN5 prefoldin subunit 5
PHF2 PHD finger protein 2
PIKFYVE phosphoinositide kinase, FYVE finger containing
PPT1 palmitoyl-protein thioesterase 1
PPT2 palmitoyl-protein thioesterase 2
PTEN phosphatase and tensin homolog
PURA purine-rich element binding protein A
RERE arginine-glutamic acid dipeptide (RE) repeats
SCN1A sodium channel, voltage gated, type I alpha subunit
SELENBP1 selenium binding protein 1
SFRP1 secreted frizzled-related protein 1
SHH sonic hedgehog
SIRT1 sirtuin 1
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SMARCA1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1
SPEF2 sperm flagellar 2
SYN2 synapsin II
TERT telomerase reverse transcriptase
TG thyroglobulin
TKT transketolase
UBE3A ubiquitin protein ligase E3A
VAMP7 vesicle-associated membrane protein 7
WWOX WW domain containing oxidoreductase
ZDHHC13 zinc finger, DHHC-type containing 13
ZDHHC17 zinc finger, DHHC-type containing 17