spred1 Phenotypes

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Phenotypes

Gene Literature (4)

Nucleotides (134)

Interactants (563)

XB-GENEPAGE-482850

Gene Symbol: spred1 Gene Name: sprouty related, EVH1 domain containing 1

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: spred1 assayed (7 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (21 sources): Abnormal sternum morphology, Attention deficit hyperactivity disorder, Axillary freckling, Cafe-au-lait spot, Downslanted palpebral fissures, Epicanthus, Generalized hypotonia, High palate, High, narrow palate, Hypertelorism, Hypotonia, Low posterior hairline, Low-set, posteriorly rotated ears, Macrocephaly, Micrognathia, Multiple lipomas, Neurofibromas, Ptosis, Short neck, Specific learning disability, Triangular face [+]
Mouse (15 sources): abnormal discrimination learning, abnormal eosinophil physiology, abnormal excitatory postsynaptic potential, abnormal spatial learning, abnormal spatial working memory, absent long term depression, craniofacial phenotype, enhanced paired-pulse facilitation, impaired swimming, increased airway responsiveness, increased mast cell degranulation, increased thigmotaxis, kinked tail, nervous system phenotype, reduced long term potentiation [+]
View all ortholog results at Monarch