atp11a Phenotypes

Phenotypes

XB-GENEPAGE-1010940

Gene Symbol: atp11a Gene Name: ATPase, class VI, type 11A

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: atp11a assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (42 sources): abnormal Meckel's cartilage morphology, abnormal Mullerian duct morphology, abnormal adenohypophysis morphology, abnormal artery morphology, abnormal bone mineralization, abnormal carotid artery morphology, abnormal coronary sinus connection, abnormal elbow joint morphology, abnormal eye muscle morphology, abnormal larynx morphology, abnormal myoblast differentiation, abnormal nasal cavity morphology, abnormal olfactory nerve morphology, abnormal optic cup morphology, abnormal optic stalk morphology, abnormal placental labyrinth vasculature morphology, abnormal skeletal muscle regeneration, abnormal thymus morphology, abnormal umbilical vein topology, abnormal vitelline vein topology, absent ductus venosus valve, absent olfactory nerve, absent pectinate muscle, additional anastomosis between intracranial vertebral arteries, aphakia, decreased bone mineral content, decreased circulating fructosamine level, dilated liver sinusoidal spaces, herniated liver, heterochrony, increased trigeminal neuroma incidence, liver hypoplasia, multiple persisting craniopharyngeal ducts, muscle phenotype, persistent trigeminal artery, placenta hemorrhage, preweaning lethality, complete penetrance, reduced sympathetic cervical ganglion size, small superior cervical ganglion, subcutaneous edema, thin myocardium compact layer, umbilical vein stenosis [+]

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Mouse (42 sources): abnormal Meckel's cartilage morphology, abnormal Mullerian duct morphology, abnormal adenohypophysis morphology, abnormal artery morphology, abnormal bone mineralization, abnormal carotid artery morphology, abnormal coronary sinus connection, abnormal elbow joint morphology, abnormal eye muscle morphology, abnormal larynx morphology, [+]