rab39b Phenotypes

Phenotypes

XB-GENEPAGE-493569

Gene Symbol: rab39b Gene Name: RAB39B, member RAS oncogene family

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: rab39b assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (57 sources): 2-3 toe syndactyly, Abnormality of movement, Attention deficit hyperactivity disorder, Autistic behavior, Babinski sign, Bilateral tonic-clonic seizure, Bradykinesia, Broad nasal tip, Clinodactyly of the 2nd toe, Cogwheel rigidity, Delayed eruption of teeth, Delayed speech and language development, Dementia, Depressed nasal bridge, Dolichocephaly, Downslanted palpebral fissures, Drooling, Dysarthria, Dyskinesia, Facial palsy, Frontal bossing, Generalized non-motor (absence) seizure, Global developmental delay, Hyperactivity, Intellectual disability, Intellectual disability, moderate, Intellectual disability, profound, Intellectual disability, severe, Lewy bodies, Long face, Long palpebral fissure, Long philtrum, Macrocephaly, Meckel diverticulum, Megalencephaly, Midface retrusion, Mild neurosensory hearing impairment, Moderate sensorineural hearing impairment, Motor stereotypy, Neurological speech impairment, Obesity, Parkinsonism, Periorbital fullness, Pes planus, Poor speech, Pyloric stenosis, Resting tremor, Rigidity, Seizure, Shortening of all distal phalanges of the fingers, Shuffling gait, Small for gestational age, Strabismus, Thick lower lip vermilion, Thin upper lip vermilion, Urinary incontinence, Widened subarachnoid space [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

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

Human (57 sources): 2-3 toe syndactyly, Abnormality of movement, Attention deficit hyperactivity disorder, Autistic behavior, Babinski sign, Bilateral tonic-clonic seizure, Bradykinesia, Broad nasal tip, Clinodactyly of the 2nd toe, Cogwheel rigidity, [+]