csnk2a1 Phenotypes

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Phenotypes

Gene Literature (5)

Nucleotides (212)

Interactants (662)

XB-GENEPAGE-959751

Gene Symbol: csnk2a1 Gene Name: casein kinase 2, alpha 1 polypeptide

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (33 sources): Abnormal heart morphology, Absent speech, Anteverted nares, Atonic seizure, Attention deficit hyperactivity disorder, Atypical behavior, Brachydactyly, Clinodactyly, Constipation, Decreased circulating IgA concentration, Decreased circulating IgG concentration, Decreased circulating immunoglobulin concentration, Delayed speech and language development, Epicanthus, Failure to thrive, Feeding difficulties, Generalized hypotonia, Global developmental delay, Highly arched eyebrow, High palate, Hypertelorism, Intellectual disability, Joint hypermobility, Low-set ears, Microcephaly, Micrognathia, Pachygyria, Ptosis, Scoliosis, Simplified gyral pattern, Synophrys, Thin upper lip vermilion, Wide nasal bridge [+]
Mouse (24 sources): abnormal eye development, abnormal heart tube morphology, abnormal limb bud morphology, abnormal neural fold elevation formation, abnormal optic stalk morphology, abnormal optic vesicle formation, abnormal otic vesicle development, abnormal pericardium morphology, abnormal surface ectoderm morphology, abnormal telencephalon development, absent heartbeat, absent mouth, decreased body length, decreased body size, decreased forebrain size, decreased hindbrain size, decreased midbrain size, dilated heart, embryonic lethality during organogenesis, incomplete penetrance, incomplete rostral neuropore closure, pericardial edema, small second pharyngeal arch, trabecula carnea hypoplasia, truncated tail bud [+]
View all ortholog results at Monarch