dlx2 Phenotypes

Phenotypes

XB-GENEPAGE-852890

Gene Symbol: dlx2 Gene Name: distal-less homeobox 2

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.
Manual annotations: dlx2 assayed (2 sources)
Computed annotations: dlx2 assayed (9 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (26 sources): abnormal alisphenoid bone morphology, abnormal basisphenoid bone morphology, abnormal cranium morphology, abnormal incudostapedial joint morphology, abnormal incus morphology, abnormal locomotor activation, abnormal mandibular nerve branching, abnormal maxilla morphology, abnormal olfactory bulb development, abnormal palatine bone morphology, abnormal pterygoid bone morphology, abnormal skeletal muscle morphology, abnormal suckling behavior, abnormal temporal bone morphology, abnormal zygomatic bone morphology, absent incus short process, absent maxillary shelf, absent palatal shelf, absent palatine bone horizontal plate, absent stapedial artery, absent stapes obturator foramen, ectopic cartilage, meteorism, neonatal lethality, complete penetrance, small pterygoid bone, small stapes [+]

Monarch Ortholog Phenotypes

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

Mouse (26 sources): abnormal alisphenoid bone morphology, abnormal basisphenoid bone morphology, abnormal cranium morphology, abnormal incudostapedial joint morphology, abnormal incus morphology, abnormal locomotor activation, abnormal mandibular nerve branching, abnormal maxilla morphology, abnormal olfactory bulb development, abnormal palatine bone morphology, [+]