Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

PDE6B

phosphodiesterase 6B, cGMP-specific, rod, beta (congenital stationary night blindness 3, autosomal dominant)CSNB3


Gene PDE6B gene interaction
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MeSH term
FrequencyCondition_Probility

Animals

80.0

Chromosome Mapping

50.0

Female

100.0

Humans

130.0

Male

100.0

Mice

30.0

Research Support, Non-U.S. Gov't

130.0

Linkage (Genetics)

40.0

Molecular Biology

20.0

Mutation

40.0

Amino Acid Sequence

40.0

Base Sequence

70.0

Cloning, Molecular

20.0

Comparative Study

30.0

DNA Mutational Analysis

30.0

Dogs

20.0

Genotype

20.0

Molecular Sequence Data

80.0

Pedigree

50.0

Polymorphism, Single-Stranded Conformational

40.0

3',5'-Cyclic-GMP Phosphodiesterase/genetics

375.0

Exons

30.0

Introns

20.0

Sequence Homology, Amino Acid

20.0

Electroretinography

21.0

Eye Proteins/*genetics

21.0

Research Support, U.S. Gov't, P.H.S.

60.0

Haplotypes

20.0

Microsatellite Repeats

30.0

*Chromosomes, Human, Pair 4

20.0

Swine/*genetics

21.0

Polymerase Chain Reaction

20.0

RNA Splicing

20.0

Phenotype

20.0

Retinitis Pigmentosa/*genetics

21.0

3',5'-Cyclic-GMP Phosphodiesterase/*genetics

318.0

Adult

20.0