lamc1 Phenotypes

Summary

Expression

Phenotypes

Gene Literature (1)

XB-GENEPAGE-478552

Gene Symbol: lamc1 Gene Name: laminin subunit gamma 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (53 sources): abnormal Cajal-Retzius cell morphology, abnormal Mullerian duct morphology, abnormal Schwann cell morphology, abnormal Wolffian duct morphology, abnormal axon radial sorting, abnormal basement membrane morphology, abnormal brain development, abnormal bronchus morphology, abnormal cerebral cortex morphology, abnormal cortical plate morphology, abnormal dorsal spinal root morphology, abnormal epididymis morphology, abnormal kidney development, abnormal lung saccule morphology, abnormal meninges morphology, abnormal neuron differentiation, abnormal peripheral nervous system regeneration, abnormal primitive endoderm morphology, abnormal quadriceps morphology, abnormal radial glial cell morphology, abnormal renal glomerular capsule morphology, abnormal renal glomerulus morphology, abnormal response to injury, abnormal sciatic nerve morphology, abnormal ventral spinal root morphology, absent metanephros, absent seminal vesicle, absent ureteric bud, absent visceral yolk sac, behavior/neurological phenotype, decreased body size, decreased brain size, decreased fetal size, decreased renal glomerulus number, decreased skeletal muscle fiber diameter, decreased skeletal muscle mass, embryo phenotype, embryonic lethality between implantation and somite formation, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, embryonic lethality, complete penetrance, forelimb paralysis, hindlimb paralysis, increased Schwann cell number, kidney microaneurysm, limb grasping, muscular atrophy, neonatal lethality, complete penetrance, no abnormal phenotype detected, reproductive system phenotype, skeletal muscle fiber atrophy, small lung, thick lung-associated mesenchyme, thin cerebral cortex [+]

Monarch Ortholog Phenotypes

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

Mouse (53 sources): abnormal Cajal-Retzius cell morphology, abnormal Mullerian duct morphology, abnormal Schwann cell morphology, abnormal Wolffian duct morphology, abnormal axon radial sorting, abnormal basement membrane morphology, abnormal brain development, abnormal bronchus morphology, abnormal cerebral cortex morphology, abnormal cortical plate morphology, [+]