sst.1 Phenotypes

Phenotypes

XB-GENEPAGE-491020

Gene Symbol: sst.1 Gene Name: somatostatin, gene 1

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: sst.1 assayed (3 sources)
Computed annotations: sst.1 assayed (15 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (29 sources): abnormal circulating alkaline phosphatase level, abnormal circulating pituitary hormone level, abnormal excitatory postsynaptic potential, abnormal gastric gland morphology, abnormal gastric parietal cell morphology, abnormal inhibitory postsynaptic potential, abnormal motor learning, abnormal stomach fundus morphology, behavior/neurological phenotype, decreased bone mineral content, decreased circulating alkaline phosphatase level, decreased circulating amylase level, decreased circulating prolactin level, decreased growth hormone level, decreased lean body mass, decreased locomotor activity, decreased startle reflex, enlarged stomach, homeostasis/metabolism phenotype, hyperchlorhydria, immune system phenotype, improved glucose tolerance, increased circulating ghrelin level, increased circulating growth hormone level, increased circulating iron level, increased susceptibility to age related obesity, increased total body fat amount, nervous system phenotype, no abnormal phenotype detected [+]

Monarch Ortholog Phenotypes

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

Mouse (29 sources): abnormal circulating alkaline phosphatase level, abnormal circulating pituitary hormone level, abnormal excitatory postsynaptic potential, abnormal gastric gland morphology, abnormal gastric parietal cell morphology, abnormal inhibitory postsynaptic potential, abnormal motor learning, abnormal stomach fundus morphology, behavior/neurological phenotype, decreased bone mineral content, [+]