Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

PKD2

polycystic kidney disease 2 (autosomal dominant)PKD4


Gene PKD2 gene interaction
View Neighborhood Gene

Result number fewer <<<< << < ALL > >> >>> more

MeSH term
FrequencyCondition_Probility

Chromatography, High Pressure Liquid

30.0

Humans

1280.0

Sensitivity and Specificity

30.0

Adolescent

140.0

Adult

270.0

Aged

170.0

Female

470.0

Genetic Screening

50.0

Genotype

120.0

Linkage (Genetics)/genetics

51.0

Male

480.0

Membrane Proteins/genetics

133.0

Middle Aged

210.0

Pedigree

280.0

Proteins/genetics

192.0

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

1030.0

Alleles

90.0

DNA/genetics

30.0

Electrophoresis, Agar Gel

20.0

Introns/genetics

20.0

Phenotype

150.0

Polymorphism, Genetic/genetics

50.0

Reverse Transcriptase Polymerase Chain Reaction

60.0

Cell Line

100.0

Enzyme Activation

20.0

Phosphorylation

40.0

Protein Kinases/*metabolism

20.0

Signal Transduction

50.0

Animals

470.0

Cell Division/genetics

20.0

DNA-Binding Proteins/genetics

20.0

Membrane Proteins/genetics/metabolism

21.0

Mice

200.0

Mice, Knockout

90.0

Mutation/genetics

70.0

Polycystic Kidney, Autosomal Dominant/*genetics/metabolism

266.0

Proteins/genetics/*metabolism

30.0

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

480.0

Calcium Channels/genetics

311.0

Comparative Study

80.0

Japan/epidemiology

20.0

Polycystic Kidney, Autosomal Dominant/*genetics

3531.0

Proteins/*genetics

211.0

Disease Models, Animal

90.0

Membrane Proteins/*genetics

323.0

Polycystic Kidney Diseases/*genetics

821.0

Child

90.0

Child, Preschool

70.0

Cysts/*genetics

250.0

Genes, Dominant

30.0

Membrane Proteins/biosynthesis/*genetics

24.0

Pregnancy

30.0

Protein Biosynthesis

30.0

Transcription, Genetic

20.0

DNA Mutational Analysis

130.0

Protein Structure, Tertiary/genetics/physiology

26.0

Signal Transduction/genetics/physiology

24.0

Amino Acid Sequence

170.0

Chromosome Mapping

100.0

Molecular Sequence Data

270.0

Organ Specificity

50.0

Sequence Analysis, DNA

70.0

Membrane Proteins/genetics/physiology

313.0

Mutation

150.0

*Alleles

20.0

Chromosomes, Human, Pair 4/*genetics

33.0

Loss of Heterozygosity/genetics

21.0

Physical Chromosome Mapping

20.0

English Abstract

70.0

Genetic Predisposition to Disease

20.0

*Linkage (Genetics)

60.0

Microsatellite Repeats/*genetics

31.0

*Polymorphism, Genetic

20.0

Linkage (Genetics)

160.0

Microsatellite Repeats

50.0

Polymerase Chain Reaction

90.0

Polymorphism, Genetic

60.0

*Evolution, Molecular

20.0

*Mutation

130.0

Polycystic Kidney, Autosomal Dominant/*genetics/pathology

457.0

*Calcium Signaling

24.0

Endoplasmic Reticulum/metabolism

20.0

Aged, 80 and over

40.0

Family Health

20.0

Genetic Heterogeneity

51.0

Genetic Markers

160.0

Korea

20.0

Lod Score

70.0

Germ-Line Mutation/genetics

34.0

Mutation/*genetics

60.0

Calcium/metabolism

40.0

Gene Expression

80.0

Membrane Proteins/genetics/*metabolism

51.0

Protein Binding

50.0

Protein Transport

30.0

Proteins/chemistry/genetics/*metabolism

22.0

Molecular Biology

20.0

Proteins/genetics/physiology

69.0

Gene Frequency

40.0

Models, Genetic

20.0

Base Sequence

170.0

Haplotypes

20.0

Heterozygote

50.0

Cell Membrane/metabolism

20.0

Polycystic Kidney, Autosomal Dominant/genetics/*metabolism

250.0

Transfection

40.0

Immunohistochemistry

60.0

Membrane Proteins/*genetics/*metabolism

24.0

Proteins/genetics/metabolism

21.0

Swine

20.0

Chromosomes, Human, Pair 16/genetics

22.0

Chromosomes, Human, Pair 4/genetics

56.0

Polymerase Chain Reaction/*methods

20.0

Polycystic Kidney, Autosomal Dominant/*genetics/physiopathology

375.0

Cell Membrane/chemistry

21.0

*Gene Expression

20.0

Glycosylation

30.0

Models, Biological

30.0

Rats

30.0

Polycystic Kidney, Autosomal Dominant/*genetics/*physiopathology

2100.0

Cloning, Molecular

90.0

Exons

60.0

Gene Expression Regulation

20.0

Introns

20.0

Mutagenesis, Site-Directed

20.0

Polycystic Kidney, Autosomal Dominant/genetics

640.0

Sequence Deletion

30.0

Sequence Homology, Nucleic Acid

30.0

Chromosomes, Human, Pair 16

32.0

Chromosomes, Human, Pair 4

43.0

Clone Cells

20.0

Exons/genetics

60.0

Polycystic Kidney, Autosomal Dominant/*genetics/*pathology

2100.0

Polymorphism, Single Nucleotide/genetics

20.0

Polymorphism, Single-Stranded Conformational

80.0

Tissue Distribution

30.0

Sequence Homology, Amino Acid

100.0

*Chromosome Mapping

40.0

Severity of Illness Index

40.0

Calcium Channels/*genetics

22.0

DNA/analysis

30.0

DNA Primers/chemistry

30.0

*Frameshift Mutation

21.0

Prognosis

20.0

Loss of Heterozygosity

40.0

Loss of Heterozygosity/*genetics

22.0

Membrane Proteins/chemistry/*genetics/metabolism

210.0

*Membrane Glycoproteins

20.0

*Phosphoproteins

21.0

Sequence Alignment

40.0

Exons/*genetics

20.0

Calcium-Binding Proteins/metabolism

22.0

*RNA Splicing

20.0

Proteins/chemistry

36.0

DNA Primers

20.0

Membrane Proteins/*genetics/metabolism

21.0

Proteins/*genetics/metabolism

31.0

*Models, Genetic

21.0

Infant, Newborn

50.0

Membrane Proteins/*physiology

21.0

Proteins/*physiology

21.0

Survival Analysis

20.0

DNA/genetics/isolation & purification

20.0

Germ-Line Mutation

30.0

Kidney/metabolism

30.0

Liver/metabolism

30.0

Blotting, Western

20.0

Polycystic Kidney, Autosomal Dominant/*metabolism

250.0

Time Factors

20.0

*Chromosomes, Human, Pair 16

31.0

*Chromosomes, Human, Pair 4

52.0

Restriction Mapping

30.0

Gene Expression Regulation/genetics

21.0

Protein Kinase C/metabolism

20.0

Kidney Failure, Chronic/etiology

311.0

Polycystic Kidney, Autosomal Dominant/*complications/genetics

2100.0

Kidney

20.0

Gene Expression/physiology

20.0

Infant

30.0

Polycystic Kidney, Autosomal Dominant/epidemiology/*genetics

240.0

Czech Republic/epidemiology

213.0

Polycystic Kidney, Autosomal Dominant/*diagnosis/epidemiology/*genetics

2100.0

Polymorphism, Restriction Fragment Length

50.0

Membrane Proteins/chemistry/*genetics

57.0

Models, Molecular

20.0

Protein Conformation

30.0

Crosses, Genetic

20.0

Recombination, Genetic

20.0

Protein Structure, Tertiary

40.0

Recombinant Fusion Proteins/metabolism

20.0

Frameshift Mutation

20.0

*Genetic Heterogeneity

21.0

DNA, Complementary

20.0

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

50.0

Chromosome Mapping/methods

21.0

Tomography, X-Ray Computed

30.0

Age of Onset

30.0

Polycystic Kidney Diseases/*diagnosis/*genetics

2100.0

Polymorphism, Genetic/*genetics

20.0

Amino Acid Substitution

30.0

Calcium/*metabolism

20.0

Mutation, Missense

20.0

Point Mutation

20.0

DNA Probes

20.0

*Variation (Genetics)

20.0

Cilia/*physiology

225.0

Receptors, Cell Surface/agonists/*metabolism

250.0

Signal Transduction/physiology

20.0