gad1.2 Phenotypes

Phenotypes

XB-GENEPAGE-5830281

Gene Symbol: gad1.2 Gene Name: glutamate decarboxylase 1 (brain, 67kDa), gene 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: gad1.2 assayed (7 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (26 sources): abnormal brain interneuron morphology, abnormal brain wave pattern, abnormal excitatory postsynaptic potential, abnormal inhibitory postsynaptic currents, abnormal involuntary movement, abnormal suckling behavior, abnormal visual cortex morphology, absent gastric milk in neonates, behavior/neurological phenotype, craniofacial phenotype, decreased gamma-aminobutyric acid level, decreased glutamate decarboxylase activity, decreased grip strength, endocrine/exocrine gland phenotype, failure of palatal shelf elevation, homeostasis/metabolism phenotype, hypoxia, lethality, complete penetrance, limb grasping, meteorism, narrow maxilla, neonatal lethality, complete penetrance, nervous system phenotype, no abnormal phenotype detected, palatal shelves fail to meet at midline, perinatal lethality, complete penetrance [+]

Monarch Ortholog Phenotypes

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

Mouse (26 sources): abnormal brain interneuron morphology, abnormal brain wave pattern, abnormal excitatory postsynaptic potential, abnormal inhibitory postsynaptic currents, abnormal involuntary movement, abnormal suckling behavior, abnormal visual cortex morphology, absent gastric milk in neonates, behavior/neurological phenotype, craniofacial phenotype, [+]