Gene Symbol
Gene Name
Aliases
Previous_Symbol
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MeSH term
Frequency
Condition_Probility
Cochlea/*metabolism
Humans
Research Support, U.S. Gov't, P.H.S.
Amino Acid Sequence
Amino Acid Substitution
Connexins/*genetics/metabolism
DNA Mutational Analysis
Erythema/*genetics
Gap Junctions/physiology
Hela Cells
Keratosis/*genetics
Molecular Sequence Data
*Mutation, Missense
Pedigree
Research Support, Non-U.S. Gov't
Sequence Alignment
Base Sequence
Deafness/*genetics
Female
Male
Polymorphism, Single-Stranded Conformational
Chromosome Mapping
Family Health
Genotype
Hearing Loss, Sensorineural/*genetics
Linkage (Genetics)
Point Mutation
Potassium Channels/*genetics
*Potassium Channels, Voltage-Gated
Animals
Mice
Rats
Mutation/*genetics
Phenotype
Reverse Transcriptase Polymerase Chain Reaction
Sequence Homology, Amino Acid
Adult
Gene Expression
Mice, Inbred C57BL
Middle Aged
Mutation
Time Factors
Connexins/*genetics
Chromosomes, Human, Pair 1
Connexins/genetics
Genes, Dominant
*Mutation
Mutation, Missense
Heteroduplex Analysis
Keratoderma, Palmoplantar/*genetics
Polymorphism, Single Nucleotide/*genetics
DNA Primers
Sequence Analysis, DNA