Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

FBN2

fibrillin 2 (congenital contractural arachnodactyly)


Gene FBN2 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Adolescent

20.0

Adult

70.0

Aged

50.0

Calcium-Binding Proteins/genetics

410.0

Child

50.0

Child, Preschool

30.0

DNA Mutational Analysis

30.0

Exons/genetics

20.0

Female

110.0

Humans

220.0

Infant

30.0

Infant, Newborn

40.0

Male

100.0

Microfilament Proteins/*genetics

118.0

Middle Aged

50.0

Phenotype

20.0

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

170.0

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

130.0

Chromosome Mapping

50.0

Marfan Syndrome/diagnosis/*genetics

228.0

*Mutation

40.0

Amino Acid Sequence

60.0

Amino Acid Substitution

20.0

Exons

20.0

Marfan Syndrome/*genetics

35.0

Molecular Sequence Data

90.0

*Point Mutation

30.0

Polymerase Chain Reaction

70.0

Polymorphism, Single-Stranded Conformational

30.0

Sequence Homology, Amino Acid

30.0

Alleles

30.0

Comparative Study

60.0

Fibroblasts

20.0

Genes, Dominant

20.0

*Chromosomes, Human, Pair 5

31.0

In Situ Hybridization, Fluorescence

20.0

Microfilament Proteins/genetics

27.0

Pregnancy

30.0

Epidermal Growth Factor/genetics

34.0

Pedigree

40.0

Base Sequence

70.0

DNA Primers

40.0

Linkage (Genetics)

20.0

Immunohistochemistry

20.0

Mutation

20.0

Cells, Cultured

20.0

Cell Line

30.0

Animals

40.0

Blotting, Northern

20.0

Cattle

20.0

Chromosomes, Human, Pair 5/*genetics

22.0

Cloning, Molecular

30.0

Extracellular Matrix Proteins/genetics

23.0

Hamsters

20.0

Microscopy, Immunoelectron

20.0

Organ Specificity

20.0

*Chromosomes, Human, Pair 15

20.0

Marfan Syndrome/genetics

317.0

Gene Frequency

20.0