rspry1 Phenotypes

Phenotypes

XB-GENEPAGE-1002343

Gene Symbol: rspry1 Gene Name: ring finger and SPRY 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: rspry1 assayed (9 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (32 sources): Abnormal facial shape, Autistic behavior, Craniosynostosis, Delayed skeletal maturation, Depressed nasal bridge, Epicanthus, Femoral bowing, Generalized hypotonia, Hypertelorism, Intellectual disability, Low-set ears, Malar flattening, Microcephaly, Microtia, Motor delay, Narrow pelvis bone, Osteopenia, Overlapping toe, Platyspondyly, Proximal femoral epiphysiolysis, Ptosis, Short femoral neck, Short metacarpal, Short neck, Short nose, Short stature, Skull asymmetry, Small epiphyses, Strabismus, Tented upper lip vermilion, Thick vermilion border, Thoracolumbar scoliosis [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

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

Human (32 sources): Abnormal facial shape, Autistic behavior, Craniosynostosis, Delayed skeletal maturation, Depressed nasal bridge, Epicanthus, Femoral bowing, Generalized hypotonia, Hypertelorism, Intellectual disability, [+]