Gene GJB6 function profile ��Ʈw

Gene Symbol

Gene Name	Aliases	Previous_Symbol
GJB6	gap junction protein, beta 6 (connexin 30)	EDH, HED, CX30, HGNC:3158	ectodermal dysplasia 2, hidrotic (Clouston syndrome)

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MeSH term

Frequency	Condition_Probility
Connexins/*genetics	19	11.0
Deafness/*genetics	13	10.0
Genes, Dominant	2	0.0
Genotype	6	0.0
*Mutation	10	0.0
Phenotype	8	0.0
Research Support, Non-U.S. Gov't	13	0.0
Amino Acid Sequence	6	0.0
Base Sequence	6	0.0
Connexins/chemistry/*genetics	2	16.0
DNA Mutational Analysis	8	0.0
Female	10	0.0
Homozygote	3	0.0
Humans	25	0.0
Male	11	0.0
Molecular Sequence Data	7	0.0
Pedigree	8	0.0
Polymorphism, Single-Stranded Conformational	2	0.0
*Gene Deletion	2	0.0
Adult	5	0.0
Child	9	0.0
Gene Deletion	3	0.0
Blotting, Southern	2	0.0
Chromosomes, Human, Pair 13	2	1.0
Genes, Recessive	3	0.0
Hearing Loss, Sensorineural/*genetics	5	5.0
Polymerase Chain Reaction	6	0.0
*Sequence Deletion	3	0.0
Animals	5	0.0
Mice	4	0.0
Mutation/*genetics	3	0.0
Research Support, U.S. Gov't, P.H.S.	6	0.0
Sequence Homology, Amino Acid	2	0.0
Syndrome	3	0.0
Alleles	3	0.0
Genes, Recessive/genetics	2	2.0
Heterozygote	7	0.0
Sequence Deletion/*genetics	2	1.0
Adolescent	4	0.0
Child, Preschool	5	0.0
Hearing Loss/*genetics	3	15.0
Middle Aged	3	0.0
Sequence Deletion	3	0.0
Gap Junctions/*genetics	2	50.0
Mutation, Missense	2	0.0
DNA/genetics	2	0.0
Gene Frequency	2	0.0