| Monarch Ortholog Phenotypes
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Human (27 sources):
Babinski sign,
Bowel incontinence,
Bowel urgency,
Cognitive impairment,
Hip dislocation,
Horseshoe kidney,
Hyperpigmentation in sun-exposed areas,
Hyperreflexia,
Kyphoscoliosis,
Lower limb muscle weakness,
Microcephaly,
Micrognathia,
Multiple lentigines,
Narrow face,
Peripheral neuropathy,
Premature graying of body hair,
Retrognathia,
Seizure,
Short stature,
Silver-gray hair,
Spastic gait,
Spastic paraplegia,
Stage 5 chronic kidney disease,
Ureteropelvic junction obstruction,
Vesicoureteral reflux,
Vitiligo,
Waddling gait
[+]
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Mouse (3 sources):
behavior/neurological phenotype,
impaired spatial learning,
nervous system phenotype
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View all ortholog results at Monarch
|
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.