Monarch Ortholog Phenotypes
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Human (69 sources):
11 pairs of ribs,
Abnormal dental enamel morphology,
Abnormal earlobe morphology,
Abnormal finger flexion creases,
Abnormal pinna morphology,
Abnormally large globe,
Absent earlobe,
Blepharophimosis,
Breast carcinoma,
Cachexia,
Carious teeth,
Cerebellar vermis hypoplasia,
Cleft palate,
Clinodactyly of the 5th finger,
Clitoral hypertrophy,
Cognitive impairment,
Cone-shaped epiphyses of the phalanges of the hand,
Cone-shaped epiphysis,
Convex nasal ridge,
Craniosynostosis,
Cryptorchidism,
Delayed skeletal maturation,
Dental crowding,
Dental malocclusion,
Dislocated radial head,
Downslanted palpebral fissures,
Elbow flexion contracture,
Enamel hypoplasia,
Facial asymmetry,
Failure to thrive,
Glaucoma,
High palate,
Hip dislocation,
Hip dysplasia,
Hyperactivity,
Hypoplasia of proximal fibula,
Hypoplasia of proximal radius,
Hypospadias,
Intellectual disability,
Intrauterine growth retardation,
Ivory epiphyses,
Large basal ganglia,
Low-set ears,
Microcephaly,
Micrognathia,
Mild global developmental delay,
Narrow face,
Pachygyria,
Pancytopenia,
Pes planus,
Prematurely aged appearance,
Prominent nose,
Proportionate short stature,
Ridged nail,
Sandal gap,
Scoliosis,
Seizure,
Selective tooth agenesis,
Short stature,
Single transverse palmar crease,
Sloping forehead,
Small anterior fontanelle,
Sparse scalp hair,
Strabismus,
Talipes equinovarus,
Telangiectasia,
Tooth agenesis,
obsolete Hypotrichosis,
obsolete Joint hyperflexibility
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Mouse (72 sources):
abnormal DNA replication,
abnormal astrocyte morphology,
abnormal bone marrow morphology,
abnormal cerebellar granule layer morphology,
abnormal cerebellum development,
abnormal cerebral cortex morphology,
abnormal embryonic/fetal subventricular zone morphology,
abnormal fontanelle morphology,
abnormal hair cycle,
abnormal hair follicle development,
abnormal hair follicle morphology,
abnormal head size,
abnormal hematopoietic stem cell morphology,
abnormal intestinal epithelium morphology,
abnormal neuron proliferation,
abnormal olfactory bulb granule cell layer morphology,
abnormal oogenesis,
abnormal placenta morphology,
abnormal primary ovarian follicle morphology,
abnormal rhombic lip morphology,
abnormal stratification in cerebral cortex,
abnormal thymus involution,
absent oocytes,
behavior/neurological phenotype,
cardiac fibrosis,
craniofacial phenotype,
decreased body length,
decreased body size,
decreased bone marrow cell number,
decreased brain size,
decreased brain weight,
decreased cell proliferation,
decreased cerebellar granule cell number,
decreased cerebellar granule cell precursor proliferation,
decreased circulating glucose level,
decreased hair follicle number,
decreased liver weight,
decreased lung weight,
decreased mitotic index,
decreased ovary weight,
decreased spleen weight,
decreased testis weight,
decreased thymocyte number,
decreased thymus weight,
delayed hair regrowth,
early cellular replicative senescence,
ectopic Purkinje cell,
embryonic lethality between implantation and somite formation, complete penetrance,
embryonic lethality prior to organogenesis,
embryonic lethality prior to tooth bud stage,
growth/size/body region phenotype,
hippocampus hypoplasia,
increased apoptosis,
increased cellular sensitivity to methylmethanesulfonate,
increased cellular sensitivity to ultraviolet irradiation,
increased fibroblast apoptosis,
increased neuron apoptosis,
increased tumor incidence,
induced chromosome breakage,
no abnormal phenotype detected,
postnatal lethality, complete penetrance,
premature aging,
premature death,
prenatal lethality, incomplete penetrance,
preweaning lethality, complete penetrance,
proportional dwarf,
renal glomerulus atrophy,
sebaceous gland hyperplasia,
small thoracic cavity,
spontaneous chromosome breakage,
thick skin,
thin epidermis
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View all ortholog results at Monarch
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