abnormal heart position or orientation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the heart is displaced from the normal left-sided position and/or orientation (Mammalian Phenotype Ontology, MP_0006065)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006065
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Genes

48 gene mutations causing the abnormal heart position or orientation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2B activin A receptor, type IIB
ANKS6 ankyrin repeat and sterile alpha motif domain containing 6
ARMC4 armadillo repeat containing 4
ATMIN ATM interactor
B9D1 B9 protein domain 1
BICC1 BicC family RNA binding protein 1
BMP2 bone morphogenetic protein 2
C1ORF127 chromosome 1 open reading frame 127
CC2D2A coiled-coil and C2 domain containing 2A
CCDC151 coiled-coil domain containing 151
CCDC39 coiled-coil domain containing 39
CFC1 cripto, FRL-1, cryptic family 1
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
DAW1 dynein assembly factor with WDR repeat domains 1
DNAAF2 dynein, axonemal, assembly factor 2
DNAAF3 dynein, axonemal, assembly factor 3
DNAH11 dynein, axonemal, heavy chain 11
DNAH5 dynein, axonemal, heavy chain 5
DNAI1 dynein, axonemal, intermediate chain 1
DRC1 dynein regulatory complex subunit 1
DYX1C1 dyslexia susceptibility 1 candidate 1
FGF10 fibroblast growth factor 10
FOXJ1 forkhead box J1
FOXP4 forkhead box P4
GDF1 growth differentiation factor 1
HOXB4 homeobox B4
INVS inversin
KIF7 kinesin family member 7
LEFTY1 left-right determination factor 1
LEFTY2 left-right determination factor 2
MAB21L2 mab-21-like 2 (C. elegans)
MEGF8 multiple EGF-like-domains 8
MGRN1 mahogunin ring finger 1, E3 ubiquitin protein ligase
MKS1 Meckel syndrome, type 1
NODAL nodal growth differentiation factor
PCSK5 proprotein convertase subtilisin/kexin type 5
PCSK6 proprotein convertase subtilisin/kexin type 6
PDLIM3 PDZ and LIM domain 3
PITX2 paired-like homeodomain 2
PKD1L1 polycystic kidney disease 1 like 1
PKD2 polycystic kidney disease 2 (autosomal dominant)
RFX3 regulatory factor X, 3 (influences HLA class II expression)
RPGRIP1L RPGRIP1-like
SOS1 son of sevenless homolog 1 (Drosophila)
TBC1D32 TBC1 domain family, member 32
TLL1 tolloid-like 1
VCL vinculin
ZIC3 Zic family member 3