dextrocardia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000644
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Genes

35 gene mutations causing the dextrocardia 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
C1ORF127 chromosome 1 open reading frame 127
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
GDF1 growth differentiation factor 1
INVS inversin
LEFTY2 left-right determination factor 2
MEGF8 multiple EGF-like-domains 8
MGRN1 mahogunin ring finger 1, E3 ubiquitin protein ligase
MKS1 Meckel syndrome, type 1
PCSK5 proprotein convertase subtilisin/kexin type 5
PCSK6 proprotein convertase subtilisin/kexin type 6
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
ZIC3 Zic family member 3