dnase1l2 Phenotypes

Summary

Expression

Phenotypes

Gene Literature (0)

XB-GENEPAGE-981739

Gene Symbol: dnase1l2 Gene Name: deoxyribonuclease I-like 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.
Computed annotations: dnase1l2 assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (47 sources): abnormal RR interval, abnormal adipose tissue amount, abnormal body length, abnormal bone mineralization, abnormal cell nucleus morphology, abnormal circulating amylase level, abnormal cranium morphology, abnormal fasting circulating glucose level, abnormal grip strength, abnormal lean body mass, abnormal locomotor activation, abnormal maxilla morphology, abnormal motor capabilities/coordination/movement, abnormal nail morphology, abnormal prepulse inhibition, abnormal spine curvature, abnormal startle reflex, abnormal tail length, abnormal tail morphology, abnormal vocalization, decreased body length, decreased bone mineral content, decreased cardiac stroke volume, decreased circulating alkaline phosphatase level, decreased circulating free fatty acids level, decreased circulating fructosamine level, decreased circulating glucose level, decreased fasting circulating glucose level, decreased grip strength, decreased hematocrit, decreased hemoglobin content, decreased lean body mass, decreased locomotor activity, decreased spleen weight, decreased startle reflex, fusion of vertebral arches, hydrometra, increased body length, increased circulating amylase level, increased fasting circulating glucose level, increased lean body mass, increased prepulse inhibition, increased total body fat amount, persistence of hyaloid vascular system, preweaning lethality, incomplete penetrance, shortened RR interval, small superior vagus ganglion [+]

Monarch Ortholog Phenotypes

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

Mouse (47 sources): abnormal RR interval, abnormal adipose tissue amount, abnormal body length, abnormal bone mineralization, abnormal cell nucleus morphology, abnormal circulating amylase level, abnormal cranium morphology, abnormal fasting circulating glucose level, abnormal grip strength, abnormal lean body mass, [+]