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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vagus nerve morphology
Debug Stats
  • ### Total Build Time: 92 ms 17.173 KB
  • CONCEPT_NAME gt=9 ms Completed: 8 ms rowSize= 390 bytes
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  • CONCEPT_GENES gt=59 ms Completed: 59 ms rowSize= 11.456 KB
  • CONCEPT_XREFS gt=10 ms Completed: 10 ms rowSize= 1.169 KB
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Jax Mouse Phenotype (1)
abnormal vagus nerve morphology MP:0001074
Definition (1)
any structural anomaly of the autonomic, sensory and motor axons of the tenth cranial nerve; it is primarily sensory but also has visceromotor components; it originates in the brain stem and controls many autonomic functions of the heart, lungs, stomach, pharynx, larynx, trachea, esophagus and other gastrointestinal tract components, and also controls some motor functions such as speech; the sensory branches mediate sensation from the pharynx, larynx, thorax and abdomen; it also innervates taste buds in the epiglottis
Synonyms (1)
"vagus nerve abnormalities" BROAD
Parents (1)
img abnormal cranial nerve morphology MP:0001056
Children (2)
img absent vagus nerve MP:0004571
img fusion of glossopharyngeal and vagus nerve MP:0004568
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal cranial nerve morphology MP:0001056
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanPLXNA491584plexin A4
Click here to display 21 evidence detail records.
HumanMESP155897mesoderm posterior 1 homolog (mouse)
Click here to display 21 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 21 evidence detail records.
HumanNKX2-826257
Click here to display 21 evidence detail records.
HumanSEMA3A10371sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
Click here to display 21 evidence detail records.
HumanPHOX2B8929paired-like homeobox 2b
Click here to display 21 evidence detail records.
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
INFERRED
HumanLMO48543LIM domain only 4
INFERRED
HumanTBX16899T-box 1
Click here to display 21 evidence detail records.
HumanSLC5A36526solute carrier family 5 (sodium/myo-inositol cotransporter), member 3
Click here to display 21 evidence detail records.
HumanHOXB33213homeobox B3
INFERRED
HumanHOXA33200homeobox A3
INFERRED
HumanHOXA23199homeobox A2
Click here to display 21 evidence detail records.
HumanHOXA13198homeobox A1
Click here to display 21 evidence detail records.
HumanGRB22885growth factor receptor-bound protein 2
Click here to display 21 evidence detail records.
HumanGBX22637gastrulation brain homeobox 2
INFERRED
HumanFBLN12192fibulin 1
Click here to display 21 evidence detail records.
HumanERBB22064v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2
Click here to display 21 evidence detail records.
HumanCLN82055ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
Click here to display 21 evidence detail records.
HumanEGR21959early growth response 2
Click here to display 21 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001074abnormal vagus nerve morphology0self