determination of left/right symmetry

determination of left/right symmetry

Item
http://www.wikidata.org/entity/Q21095348
Sonic hedgehogActivin A receptor, type ICActivin A receptor, type 1Activin receptor IIAActivin receptor IIBCripto, FRL-1, cryptic family 1Forkhead box H1ADP ribosylation factor like GTPase 6Forkhead box J1Kinesin family member 3BCoiled-coil domain containing 151Coiled-coil domain containing 103Cilia and flagella associated protein 53Chromosome 9 open reading frame 116Dynein cytoplasmic 2 heavy chain 1Regulatory factor X3Polycystin 2, transient receptor potential cation channelMcKusick-Kaufman syndromeDishevelled associated activator of morphogenesis 2Dynein axonemal assembly factor 4Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 2ADP ribosylation factor like GTPase 13BPaired like homeodomain 2Forkhead box F1Axin 1Adaptor related protein complex 1 subunit beta 1STIL centriolar assembly proteinDynein cytoplasmic 2 light intermediate chain 1Dynein axonemal intermediate chain 2Dynein axonemal intermediate chain 1TBC1 domain family member 32Coiled-coil and C2 domain containing 2AGrowth arrest specific 8Dispatched RND transporter family member 1Bardet-Biedl syndrome 7Multiple EGF like domains 8Cripto, FRL-1, cryptic family 1Deleted in primary ciliary dyskinesia homolog (mouse)Dynein axonemal heavy chain 5Dynein axonemal heavy chain 11
P682
Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor proteinLoss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defectsMutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructurePrimary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutationsMutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia.Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesiaHigh prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebratesA human laterality disorder caused by a homozygous deleterious mutation in MMP21A Zebrafish Loss-of-Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ Function
P921
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P682

determination of left/right symmetry

Item
http://www.wikidata.org/entity/Q21095348
description
The establishment of an organi ...... n deviates from this symmetry.
@en
biologisch proces
@nl
name
determination of left/right symmetry
@en
determinering av venstre-høgre-symmetri
@nn
type
label
determination of left/right symmetry
@en
determinering av venstre-høgre-symmetri
@nn
altLabel
GO:0007368
@en
determination of left/right asymmetry
@en
determinering av venstre-høgre-asymmetri
@nn
prefLabel
determination of left/right symmetry
@en
determinering av venstre-høgre-symmetri
@nn
P279
P2888
P31
P686
P279
P2888
P31
P686