kat2a Phenotypes

Phenotypes

XB-GENEPAGE-992486

Gene Symbol: kat2a Gene Name: K(lysine) acetyltransferase 2A

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: kat2a manipulated (1 source)

Experiments (Reagents) These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + kat2a KD (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (41 sources): abnormal breathing pattern, abnormal cerebellum vermis morphology, abnormal chordamesoderm morphology, abnormal embryo development, abnormal embryonic growth/weight/body size, abnormal extraembryonic coelom morphology, abnormal head mesenchyme morphology, abnormal mesoderm development, abnormal paraxial mesoderm morphology, abnormal sternebra number, abnormal telencephalon development, abnormal vitelline vasculature morphology, absent notochord, absent somites, behavior/neurological phenotype, decreased body size, decreased embryo size, decreased fetal size, decreased fibroblast proliferation, decreased lumbar vertebrae number, embryo phenotype, embryonic growth arrest, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, embryonic lethality, complete penetrance, failure of somite differentiation, hunched posture, incomplete rostral neuropore closure, increased embryonic tissue cell apoptosis, lumbar vertebral transformation, nervous system phenotype, no abnormal phenotype detected, open neural tube, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, respiratory system phenotype, skeleton phenotype, small xiphoid process, thoracic vertebral transformation, vertebral transformation [+]

Monarch Ortholog Phenotypes

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

Mouse (41 sources): abnormal breathing pattern, abnormal cerebellum vermis morphology, abnormal chordamesoderm morphology, abnormal embryo development, abnormal embryonic growth/weight/body size, abnormal extraembryonic coelom morphology, abnormal head mesenchyme morphology, abnormal mesoderm development, abnormal paraxial mesoderm morphology, abnormal sternebra number, [+]