Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

APOC2

apolipoprotein C-II


Gene APOC2 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Alleles

120.0

Chromosome Mapping

130.0

Comparative Study

40.0

Female

360.0

*Genome, Human

20.0

Genotype

40.0

Humans

640.0

Linkage (Genetics)

140.0

Lod Score

101.0

Male

350.0

Microsatellite Repeats

40.0

Pedigree

230.0

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

500.0

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

160.0

China

20.0

*Chromosome Mapping

60.0

Chromosomes, Human, Pair 6/genetics

21.0

Cleft Lip/*genetics

34.0

Cleft Palate/*genetics

34.0

Genetic Markers/genetics

20.0

Statistics

20.0

*Transcription Factors

20.0

Animals

100.0

Adult

110.0

Predictive Value of Tests

20.0

Pregnancy

60.0

Apolipoproteins C/*genetics

1112.0

Apolipoproteins E/*genetics

50.0

Molecular Sequence Data

90.0

*Multigene Family

40.0

Cell Line

50.0

Mice

50.0

Mice, Transgenic

20.0

Aged

50.0

Aged, 80 and over

30.0

Genetic Markers

200.0

Apolipoproteins E/genetics

30.0

European Continental Ancestry Group/*genetics

20.0

Gene Frequency

90.0

*Haplotypes

20.0

Adolescent

30.0

Apolipoproteins/blood

20.0

Child

40.0

Lipoproteins, HDL Cholesterol/blood

20.0

Chromosome Mapping/*methods

21.0

Linkage Disequilibrium

20.0

Middle Aged

40.0

Blood Group Antigens/genetics

23.0

Genetic Markers/*genetics

21.0

Phenotype

20.0

Base Sequence

70.0

*Chromosomes, Human, Pair 19

227.0

DNA/blood/genetics

23.0

Polymerase Chain Reaction

70.0

Polymorphism, Genetic

90.0

*Linkage (Genetics)

171.0

Amino Acid Sequence

20.0

*Genes, Structural

30.0

Blood Proteins/*genetics

31.0

*Genetics, Population

20.0

*Polymorphism, Genetic

40.0

*Variation (Genetics)

30.0

Gene Frequency/genetics

20.0

Heterozygote Detection

20.0

Chromosome Banding

20.0

Recombination, Genetic

40.0

Software

20.0

Haplotypes

40.0

Linkage Disequilibrium/*genetics

22.0

Myotonic Dystrophy/epidemiology/*genetics

250.0

*Polymorphism, Restriction Fragment Length

50.0

Polymorphism, Restriction Fragment Length

80.0

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

30.0

Risk Factors

30.0

*Repetitive Sequences, Nucleic Acid

20.0

Restriction Mapping

20.0

Blotting, Southern

20.0

DNA Probes

30.0

Myotonic Dystrophy/*diagnosis/genetics

360.0

Hybrid Cells

70.0

Myotonic Dystrophy/*genetics

1320.0

DNA/analysis

20.0

Myotonic Dystrophy/diagnosis/*genetics

266.0

*Genetic Markers

41.0

*Prenatal Diagnosis

20.0

Chromosomes, Human, Pair 19

52.0

Apolipoproteins C/genetics

617.0

Genetic Markers/analysis

27.0

Isoenzymes

31.0

Creatine Kinase/*genetics

420.0

*DNA Repair

20.0

Dogs

20.0

Hamsters

30.0

Muscles/*enzymology

22.0

Myotonic Dystrophy/enzymology/*genetics

220.0

Translocation, Genetic

20.0

Apolipoproteins/*genetics

22.0

Nucleic Acid Hybridization

20.0

Complement 3/genetics

25.0

*Chromosomes, Human, 19-20

418.0

Dipeptidases/*genetics

222.0

DNA Restriction Enzymes

30.0