Gene USH2A function profile ��Ʈw

Gene Symbol

Gene Name	Aliases	Previous_Symbol
USH2A	Usher syndrome 2A (autosomal recessive, mild)

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MeSH term

Frequency	Condition_Probility
DNA/chemistry/genetics	2	0.0
DNA Mutational Analysis	4	0.0
Extracellular Matrix Proteins/*genetics	8	10.0
Humans	23	0.0
Mutation	4	0.0
Polymorphism, Single-Stranded Conformational	2	0.0
Research Support, Non-U.S. Gov't	19	0.0
Spain	2	0.0
Syndrome	16	0.0
Adult	5	0.0
Alleles	2	0.0
Female	8	0.0
Genetic Markers/genetics	2	0.0
Linkage (Genetics)/genetics	2	0.0
Male	8	0.0
Pedigree	8	0.0
Research Support, U.S. Gov't, P.H.S.	11	0.0
Animals	4	0.0
Chromosome Mapping	7	0.0
Linkage (Genetics)	4	0.0
Genes, Recessive	2	0.0
Hearing Loss, Sensorineural/*genetics	4	4.0
Mutation/*genetics	3	0.0
Retinitis Pigmentosa/*genetics	6	4.0
Adolescent	3	0.0
*Chromosome Mapping	2	0.0
Polymerase Chain Reaction	2	0.0
Retinal Degeneration/*genetics	2	5.0
Genetic Heterogeneity	2	0.0
Middle Aged	2	0.0
Retinitis Pigmentosa/genetics	2	8.0
Mice	2	0.0
Cross-Sectional Studies	2	0.0
Lod Score	2	0.0
Amino Acid Sequence	5	0.0
Chromosomes, Human, Pair 1	2	0.0
Gene Expression	2	0.0
Molecular Sequence Data	5	0.0
Genotype	3	0.0
Phenotype	3	0.0
Base Sequence	5	0.0
In Situ Hybridization, Fluorescence	2	0.0
Sequence Alignment	2	0.0
Comparative Study	2	0.0