Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

OPA1

optic atrophy 1 (autosomal dominant)NTG, KIAA0567, FLJ12460, NPG, largeG


Gene OPA1 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

GTP Phosphohydrolases/*genetics

1336.0

Humans

400.0

Intraocular Pressure/*genetics

2100.0

Mutation/genetics

30.0

Polymerase Chain Reaction

90.0

Polymorphism, Genetic/*genetics

20.0

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

370.0

Adult

140.0

Base Sequence

70.0

Child

110.0

Male

230.0

Molecular Sequence Data

120.0

*Mutation

50.0

Pedigree

200.0

Visual Acuity

42.0

Adolescent

110.0

Aged

90.0

Child, Preschool

50.0

DNA Mutational Analysis

70.0

GTP Phosphohydrolases/*genetics/metabolism

337.0

Genotype

80.0

Middle Aged

130.0

Phenotype

50.0

Polymorphism, Genetic

50.0

Polymorphism, Single-Stranded Conformational

30.0

Animals

80.0

*Chromosomes, Human, Pair 3

71.0

Optic Atrophy, Autosomal Dominant/*genetics

3100.0

Sequence Deletion

30.0

Amino Acid Sequence

40.0

Dynamins

24.0

Mice

60.0

Mice, Inbred BALB C

20.0

Point Mutation

20.0

Sequence Alignment

20.0

Sequence Homology, Amino Acid

30.0

Genetic Markers

60.0

Optic Nerve/metabolism

240.0

*Polymorphism, Genetic

20.0

Mutation, Missense

20.0

DNA/chemistry/genetics

20.0

Family Health

20.0

Female

220.0

Gene Frequency

30.0

Haplotypes

60.0

Microsatellite Repeats

20.0

Mutation

30.0

Optic Atrophies, Hereditary/diagnosis/*genetics

360.0

Alleles

40.0

Genes, Dominant/*genetics

55.0

Optic Atrophies, Hereditary/*genetics

1155.0

Sequence Tagged Sites

31.0

Chromosome Mapping

90.0

Chromosomes, Artificial, Yeast

30.0

Cloning, Molecular

20.0

Expressed Sequence Tags

20.0

*Founder Effect

21.0

Genetic Markers/genetics

20.0

Chromosomes, Human, Pair 3/genetics

53.0

Linkage (Genetics)

30.0

Perimetry

27.0

*Chromosome Mapping

70.0

Disease Models, Animal

20.0

Mice, Inbred C57BL

30.0

Mice, Mutant Strains

20.0

Retinal Ganglion Cells/*metabolism

266.0

Genetic Heterogeneity

31.0

Case-Control Studies

20.0

*Drosophila Proteins

20.0

*Genes, Dominant

20.0

English Abstract

20.0

*Linkage (Genetics)

30.0

Chromosomes, Human, Pair 3/*genetics

62.0

Genes, Dominant

40.0

DNA Primers

20.0

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

40.0

Lod Score

30.0

Repetitive Sequences, Nucleic Acid

20.0

Aged, 80 and over

20.0

Linkage (Genetics)/*genetics

20.0

Hela Cells

20.0

RNA, Messenger/metabolism

20.0

Blotting, Western

20.0

Rats

20.0