fgfrl1 Phenotypes

Summary

Expression

Phenotypes

XB-GENEPAGE-482471

Gene Symbol: fgfrl1 Gene Name: fibroblast growth factor receptor like 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: fgfrl1 assayed (5 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (57 sources): abnormal atrioventricular valve morphology, abnormal cervical atlas morphology, abnormal cervical vertebrae morphology, abnormal diaphragm development, abnormal erythroblast number, abnormal foramen magnum morphology, abnormal forebrain development, abnormal kidney development, abnormal metanephric mesenchyme morphology, abnormal metanephros morphology, abnormal nephrogenic mesenchyme morphogenesis, abnormal neurocranium morphology, abnormal occipital bone morphology, abnormal semilunar valve morphology, abnormal sphenoid bone morphology, abnormal sternum ossification, abnormal vascular development, abnormal vitelline vasculature morphology, absent metanephros, absent nephron, axial skeleton hypoplasia, cardiac valve regurgitation, decreased birth body size, decreased erythrocyte cell number, decreased hematocrit, decreased hemoglobin content, decreased hyoid bone size, decreased kidney cell proliferation, decreased long bone epiphyseal plate size, decreased renal glomerulus number, delayed cranial suture closure, disorganized placental labyrinth, domed cranium, fetal growth retardation, fusion of basioccipital and basisphenoid bone, homeostasis/metabolism phenotype, impaired branching involved in ureteric bud morphogenesis, increased kidney apoptosis, lethality throughout fetal growth and development, incomplete penetrance, mandible hypoplasia, muscle phenotype, neonatal lethality, complete penetrance, no abnormal phenotype detected, no spontaneous movement, pale placenta, respiratory system phenotype, skeleton phenotype, small basioccipital bone, small basisphenoid bone, small cranium, small cricoid cartilage, small thoracic cage, small thoracic cavity, small thyroid cartilage, thin diaphragm muscle, thin myocardium, thin neurocranium [+]

Monarch Ortholog Phenotypes

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

Mouse (57 sources): abnormal atrioventricular valve morphology, abnormal cervical atlas morphology, abnormal cervical vertebrae morphology, abnormal diaphragm development, abnormal erythroblast number, abnormal foramen magnum morphology, abnormal forebrain development, abnormal kidney development, abnormal metanephric mesenchyme morphology, abnormal metanephros morphology, [+]