syp Phenotypes

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PhenotypesPheno.

Gene Literature (19)Lit. (19)

GO Terms (58)GO (58)

Nucleotides (297)Nucl. (297)

Proteins (44)Prot. (44)

Interactants (352)Interact. (352)

XB-GENEPAGE-943860

Gene Symbol: syp Gene Name: synaptophysin

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: syp assayed (4 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (38 sources): 2-3 toe syndactyly, Attention deficit hyperactivity disorder, Autistic behavior, Babinski sign, Bilateral tonic-clonic seizure, Broad nasal tip, Clinodactyly of the 2nd toe, Delayed eruption of teeth, Delayed speech and language development, Depressed nasal bridge, Downslanted palpebral fissures, Drooling, Facial palsy, Generalized non-motor (absence) seizure, Global developmental delay, Intellectual disability, Long palpebral fissure, Long philtrum, Macrocephaly, Meckel diverticulum, Midface retrusion, Mild neurosensory hearing impairment, Moderate intellectual disability, Moderate sensorineural hearing impairment, Obesity, Periorbital fullness, Pes planus, Poor speech, Profound intellectual disability, Pyloric stenosis, Seizure, Severe intellectual disability, Shortening of all distal phalanges of the fingers, Small for gestational age, Thick lower lip vermilion, Thin upper lip vermilion, Urinary incontinence, Widened subarachnoid space [+]
Mouse (1 source): no abnormal phenotype detected
View all ortholog results at Monarch