kif3a Phenotypes

Summary

Expression

Phenotypes

XB-GENEPAGE-986463

Gene Symbol: kif3a Gene Name: kinesin family member 3A

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: kif3a assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (58 sources): abnormal actin cytoskeleton morphology, abnormal basicranium morphology, abnormal basisphenoid bone morphology, abnormal chondrocyte morphology, abnormal cranial neural crest cell morphology, abnormal craniofacial bone morphology, abnormal craniofacial development, abnormal cranium morphology, abnormal developmental patterning, abnormal direction of heart looping, abnormal embryo turning, abnormal endochondral bone ossification, abnormal frontal bone morphology, abnormal heart looping, abnormal left-right axis patterning, abnormal limb bud morphology, abnormal limb development, abnormal long bone epiphyseal plate morphology, abnormal long bone epiphyseal plate proliferative zone, abnormal long bone hypertrophic chondrocyte zone, abnormal maxilla morphology, abnormal mesoderm development, abnormal nasal bone morphology, abnormal nasal septum morphology, abnormal palatine bone morphology, abnormal photoreceptor inner segment morphology, abnormal primitive node morphology, abnormal somite development, absent embryonic cilia, absent kidney epithelial cell primary cilium, absent mandibular condyloid process, absent mandibular ramus, absent nodal flow, anterior cranium occultum, broad frontonasal prominence, caudal body truncation, decreased body size, decreased embryo size, decreased long bone epiphyseal plate size, delayed heart looping, disorganized long bone epiphyseal plate, disproportionate dwarf, distended pericardium, embryonic lethality during organogenesis, complete penetrance, incomplete embryo turning, increased cranial neural crest cell proliferation, increased kidney apoptosis, kidney medulla cyst, myocardium hypoplasia, neural tube degeneration, pericardial edema, retina photoreceptor degeneration, short mandible, short photoreceptor inner segment, short photoreceptor outer segment, situs inversus, small pharyngeal arch, wavy neural tube [+]

Monarch Ortholog Phenotypes

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

Mouse (58 sources): abnormal actin cytoskeleton morphology, abnormal basicranium morphology, abnormal basisphenoid bone morphology, abnormal chondrocyte morphology, abnormal cranial neural crest cell morphology, abnormal craniofacial bone morphology, abnormal craniofacial development, abnormal cranium morphology, abnormal developmental patterning, abnormal direction of heart looping, [+]