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Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

ATP7B

ATPase, Cu++ transporting, beta polypeptide (Wilson disease)


Gene ATP7B gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Animals

400.0

Cation Transport Proteins/*metabolism

337.0

Copper/*metabolism

2527.0

Humans

1160.0

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

780.0

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

230.0

Adenosinetriphosphatase/*genetics

3030.0

Cation Transport Proteins/*genetics

1132.0

Copper/metabolism

1726.0

Gene Therapy

20.0

Liver/pathology

21.0

Microscopy, Fluorescence

40.0

Rats

130.0

Rats, Inbred LEC

457.0

Reverse Transcriptase Polymerase Chain Reaction

80.0

Adult

200.0

Base Sequence

210.0

DNA Mutational Analysis

160.0

Female

380.0

Gene Frequency

60.0

Haplotypes

50.0

Hepatolenticular Degeneration/*genetics

1970.0

Male

260.0

*Mutation

140.0

Adenosinetriphosphatase/*genetics/metabolism

726.0

Aged

40.0

Aged, 80 and over

20.0

*Arabidopsis Proteins

22.0

Cation Transport Proteins/*genetics/metabolism

360.0

Immunoenzyme Techniques

20.0

Middle Aged

40.0

*Neoplasm Proteins

20.0

RNA, Messenger/metabolism

20.0

Tumor Cells, Cultured

110.0

Adolescent

150.0

Ceruloplasmin/analysis

310.0

Child

140.0

China

20.0

Mutation

180.0

Adenosinetriphosphatase/*chemistry/genetics/metabolism

266.0

Cation Transport Proteins/*chemistry/genetics/metabolism

2100.0

Proteasome Endopeptidase Complex

20.0

Protein Conformation

30.0

Adenosinetriphosphatase/*biosynthesis

250.0

Antineoplastic Agents/*pharmacology

30.0

Cation Transport Proteins/*biosynthesis

266.0

Cisplatin/*pharmacology

43.0

Drug Resistance, Neoplasm

61.0

Drug Screening Assays, Antitumor

20.0

RNA, Messenger/analysis

20.0

English Abstract

90.0

Exons/genetics

20.0

Gene Deletion

20.0

Hepatolenticular Degeneration/epidemiology/*genetics

2100.0

Point Mutation/*genetics

20.0

Polymerase Chain Reaction

130.0

Carrier Proteins/*genetics

181.0

*Cation Transport Proteins

4922.0

Exons

100.0

Polymorphism, Single-Stranded Conformational

110.0

Chelating Agents/therapeutic use

228.0

Copper

315.0

Homozygote

40.0

Sequence Analysis, DNA

30.0

CHO Cells

50.0

Fluorescent Antibody Technique

70.0

Hamsters

80.0

Hepatolenticular Degeneration/*genetics/metabolism

4100.0

Sheep

30.0

Transfection

70.0

Adenosinetriphosphatase/*chemistry/genetics/*metabolism

360.0

Carrier Proteins/*chemistry/genetics/*metabolism

24.0

Copper/metabolism/*pharmacology

450.0

Kinetics

50.0

Menkes Kinky Hair Syndrome/*genetics

418.0

Models, Molecular

50.0

Phosphorylation

30.0

Plasmids

20.0

Protein Structure, Secondary

40.0

*Recombinant Fusion Proteins

1118.0

Genotype

130.0

Phenotype

100.0

Adenosinetriphosphatase/*analysis

2100.0

*Chromosome Deletion

20.0

Carrier Proteins/*genetics/metabolism

41.0

Cell Line

30.0

Microscopy, Confocal

20.0

Microscopy, Electron

20.0

Mutation/*physiology

21.0

Tissue Distribution

50.0

Adenosinetriphosphatase/genetics/metabolism

312.0

Carrier Proteins/genetics/metabolism

21.0

Hepatolenticular Degeneration/*genetics/*metabolism

2100.0

Homeostasis

41.0

Iron/*metabolism

21.0

Alleles

30.0

DNA/analysis

30.0

DNA Mutational Analysis/methods

20.0

*Gene Frequency

20.0

*Polymorphism, Single Nucleotide

20.0

Hepatolenticular Degeneration/genetics/metabolism

375.0

Menkes Kinky Hair Syndrome/genetics

360.0

Mice

120.0

Mice, Inbred BALB C

30.0

Disease Models, Animal

50.0

Liver/metabolism

20.0

*Gene Deletion

30.0

Polymorphism, Genetic/genetics

20.0

Adenosinetriphosphatase/genetics

614.0

Carrier Proteins/genetics

51.0

Hepatolenticular Degeneration/ethnology/*genetics

2100.0

*Mutation, Missense

30.0

Pedigree

60.0

Taiwan

21.0

Adenosinetriphosphatase/*metabolism

37.0

Biological Transport/drug effects

20.0

Cell Membrane/metabolism

20.0

Golgi Apparatus/metabolism

63.0

Adenosinetriphosphatase/genetics/*metabolism

310.0

Hepatolenticular Degeneration/enzymology/genetics

266.0

Recombinant Fusion Proteins/metabolism

30.0

Amino Acid Substitution

40.0

Ceruloplasmin/metabolism

311.0

Fluorescent Antibody Technique, Indirect

20.0

Hela Cells

20.0

Mutagenesis, Site-Directed

60.0

Amino Acid Sequence

120.0

Binding Sites

50.0

Circular Dichroism

20.0

Hepatolenticular Degeneration/*metabolism

360.0

Molecular Sequence Data

180.0

Protein Structure, Tertiary

40.0

Zinc/metabolism

22.0

Antineoplastic Agents/pharmacology

20.0

Biological Transport

90.0

Blotting, Western

60.0

Cell Line, Tumor

30.0

Cloning, Molecular

50.0

Dose-Response Relationship, Drug

20.0

Protein Binding

30.0

Time Factors

20.0

Polymerase Chain Reaction/methods

20.0

DNA Transposable Elements

21.0

Frameshift Mutation

41.0

Japan

40.0

Mutation, Missense

30.0

Sequence Deletion

60.0

Comparative Study

70.0

Liver/*metabolism

30.0

Carcinoma, Hepatocellular

20.0

Cells, Cultured

40.0

Heterozygote Detection

30.0

Introns

30.0

Polymorphism, Genetic

30.0

Chromosome Mapping

60.0

*Disease Models, Animal

51.0

Dog Diseases/*genetics/metabolism

240.0

Hepatolenticular Degeneration/genetics

880.0

*Molecular Chaperones

21.0

Pseudogenes

21.0

Sequence Alignment

40.0

Sequence Homology, Amino Acid

20.0

Species Specificity

20.0

Adenosinetriphosphatase/*chemistry/*genetics

250.0

Cation Transport Proteins/*chemistry/*genetics

2100.0

Protein Folding

30.0

Temperature

20.0

Immunohistochemistry

70.0

Menkes Kinky Hair Syndrome/genetics/*metabolism

266.0

Mutagenesis, Insertional

20.0

Heterozygote

30.0

Sensitivity and Specificity

20.0

Dogs

40.0

DNA Primers

50.0

In Situ Hybridization, Fluorescence

20.0

*Saccharomyces cerevisiae Proteins

30.0

Gene Expression

20.0

DNA Primers/genetics

30.0

Age of Onset

30.0

DNA, Complementary/genetics

30.0

Genetic Complementation Test

30.0

Iron/metabolism

21.0

Recombinant Fusion Proteins/immunology

21.0

Cell Compartmentation

20.0

Fibroblasts

30.0

Models, Statistical

21.0

Blotting, Northern

20.0

Pregnancy

30.0

Mutagenesis

40.0

Retrospective Studies

20.0

DNA, Complementary

20.0

Point Mutation

50.0

Recombinant Proteins/chemistry/metabolism

20.0

Adenosine Triphosphate/metabolism

20.0

Menkes Kinky Hair Syndrome/genetics/metabolism

3100.0

Hepatolenticular Degeneration/enzymology/*genetics

266.0

Adenosinetriphosphatase/metabolism

43.0

Polymorphism, Restriction Fragment Length

20.0

RNA Splicing

30.0

Prognosis

20.0

In Situ Hybridization/methods

21.0

Cation Transport Proteins/genetics

212.0

Repetitive Sequences, Nucleic Acid

20.0

*DNA Mutational Analysis

21.0

Italy/ethnology

25.0

Restriction Mapping

20.0

Mice, Mutant Strains

30.0

Cation Transport Proteins/metabolism

330.0

*Exons

20.0

Binding Sites/genetics

20.0

Child, Preschool

40.0

Mutation/*genetics

40.0

*Drug Resistance, Neoplasm

21.0

Green Fluorescent Proteins

20.0

Reference Values

20.0

Cation Transport Proteins/genetics/*metabolism

216.0

Survival Rate

20.0

Adenosinetriphosphatase/*genetics/*metabolism

228.0

Cation Transport Proteins/*genetics/*metabolism

225.0

Subcellular Fractions/enzymology

22.0