wnt9a Phenotypes

Phenotypes

XB-GENEPAGE-5895366

Gene Symbol: wnt9a Gene Name: wingless-type MMTV integration site family member 9A

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: wnt9a assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (13 sources): abnormal basioccipital bone morphology, abnormal cervical atlas morphology, abnormal chondrocyte physiology, abnormal cranium morphology, abnormal frontal bone morphology, abnormal interfrontal bone morphology, abnormal sagittal suture morphology, abnormal skeleton development, abnormal supraoccipital bone morphology, ectopic cartilage, hyoid bone hypoplasia, neonatal lethality, complete penetrance, small basioccipital bone [+]

Monarch Ortholog Phenotypes

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

Mouse (13 sources): abnormal basioccipital bone morphology, abnormal cervical atlas morphology, abnormal chondrocyte physiology, abnormal cranium morphology, abnormal frontal bone morphology, abnormal interfrontal bone morphology, abnormal sagittal suture morphology, abnormal skeleton development, abnormal supraoccipital bone morphology, ectopic cartilage, [+]