Gene GJB1 function profile ��Ʈw

Gene Symbol

Gene Name	Aliases	Previous_Symbol
GJB1	gap junction protein, beta 1, 32kDa (connexin 32, Charcot-Marie-Tooth neuropathy, X-linked)	CX32	gap junction protein, beta 1, 32kD (connexin 32, Charcot-Marie-Tooth neuropathy, X-linked)

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MeSH term

Frequency	Condition_Probility
Connexins/genetics/metabolism	2	100.0
Humans	31	0.0
Phenotype	6	0.0
Research Support, Non-U.S. Gov't	25	0.0
Research Support, U.S. Gov't, P.H.S.	8	0.0
Amino Acid Sequence	5	0.0
Base Sequence	6	0.0
Connexins/chemistry/*genetics	2	16.0
DNA Mutational Analysis	8	0.0
Deafness/*genetics	3	2.0
Female	12	0.0
Male	14	0.0
Molecular Sequence Data	6	0.0
Pedigree	8	0.0
Polymorphism, Single-Stranded Conformational	3	0.0
Protein Structure, Tertiary	2	0.0
Animals	9	0.0
Mice	5	0.0
Mutation/*genetics	4	0.0
Polymerase Chain Reaction	3	0.0
Sequence Homology, Amino Acid	2	0.0
Adolescent	4	0.0
Adult	6	0.0
Connexins/genetics	4	8.0
Linkage (Genetics)	4	0.0
Mutation	3	0.0
X Chromosome/*genetics	2	0.0
Charcot-Marie-Tooth Disease/*genetics	8	5.0
DNA Mutational Analysis/*methods	2	1.0
Myelin Proteins/genetics	2	3.0
Amino Acid Substitution	2	0.0
Genes, Dominant	3	0.0
Chromosomes, Human, Pair 17/*genetics	2	1.0
Gene Duplication	3	1.0
Genetic Screening	2	0.0
Genotype	2	0.0
Hereditary Motor and Sensory Neuropathies/*genetics	2	4.0
Myelin P0 Protein/genetics	2	13.0
Child	2	0.0
Connexins/*genetics	11	6.0
Myelin P0 Protein/*genetics	3	10.0
*Point Mutation	2	0.0
*Mutation	4	0.0
Rats	2	0.0
English Abstract	3	0.0
Mice, Inbred C57BL	2	0.0
Middle Aged	2	0.0
Myelin Proteins/*genetics	3	2.0
Charcot-Marie-Tooth Disease/genetics	2	8.0
*X Chromosome	7	0.0
Chromosome Mapping	3	0.0
Blotting, Southern	4	0.0
Connexins	4	66.0
Hybrid Cells	3	0.0
Membrane Proteins/*genetics	4	0.0
Axons/pathology	2	6.0