Gene Symbol
Gene Name
Aliases
Previous_Symbol
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MeSH term
Frequency
Condition_Probility
Adult
Ca(2+)-Transporting ATPase/*genetics
Female
Gene Deletion
Genotype
Humans
Male
Middle Aged
Mutation, Missense
Pemphigus, Benign Familial/*genetics
Phenotype
Research Support, Non-U.S. Gov't
Codon, Nonsense
RNA Splice Sites/genetics
Animals
Ca(2+)-Transporting ATPase/genetics/*physiology
Calcium/metabolism
Mutation
Amino Acid Sequence
Molecular Sequence Data
*Mutation
Pemphigus, Benign Familial/*genetics/pathology
Ca(2+)-Transporting ATPase/*genetics/metabolism
Golgi Apparatus/*metabolism
Cells, Cultured
Keratinocytes/cytology/*metabolism
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, U.S. Gov't, P.H.S.