Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

A B C D E F G H I J K L M N O P Q R X Y Z



Gene Symbol
Gene NameAliasesPrevious_Symbol

FOXC2

forkhead box C2 (MFH-1, mesenchyme forkhead 1)MFH-1


Gene FOXC2 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Adolescent

40.0

Adult

80.0

Child

50.0

Child, Preschool

20.0

DNA-Binding Proteins/*genetics

90.0

Female

130.0

Humans

270.0

Infant

30.0

Linkage (Genetics)/*genetics

20.0

Male

140.0

Phenotype

70.0

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

200.0

Syndrome

40.0

Transcription Factors/*genetics

100.0

Adipocytes/*metabolism

24.0

Animals

110.0

Mice

100.0

Aged

20.0

Aged, 80 and over

20.0

DNA Mutational Analysis

40.0

Eyelashes/*abnormalities

2100.0

Family Health

20.0

Middle Aged

60.0

Mutation

20.0

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

120.0

Blotting, Northern

20.0

Insulin Resistance/*genetics

22.0

Mice, Inbred C57BL

20.0

Mice, Transgenic

40.0

Cells, Cultured

30.0

Comparative Study

20.0

DNA-Binding Proteins/*genetics/metabolism

20.0

Disease Models, Animal

30.0

In Situ Hybridization

30.0

Mice, Mutant Strains

40.0

Transcription Factors/*genetics/metabolism

20.0

Base Sequence

60.0

Chromosomes, Human, Pair 16/genetics

22.0

Cleft Palate/genetics

312.0

Lymphedema/*genetics

266.0

Molecular Sequence Data

60.0

Mutation/*genetics

20.0

Polymerase Chain Reaction

20.0

Genotype

30.0

Germany

20.0

Pedigree

50.0

DNA-Binding Proteins/*genetics/physiology

33.0

Heterozygote

40.0

Intraocular Pressure/genetics

250.0

Transcription Factors/*genetics/physiology

33.0

Gene Expression Regulation, Developmental

20.0

Homozygote

20.0

Mice, Knockout

20.0

Models, Biological

20.0

DNA Primers

20.0

Glucose Tolerance Test

20.0

Reverse Transcriptase Polymerase Chain Reaction

20.0

Genes, Dominant

20.0

Lymphatic Abnormalities/genetics/pathology

2100.0

Adipocytes/metabolism

24.0

Muscle, Skeletal/metabolism

21.0

Signal Transduction/*physiology

20.0

Amino Acid Sequence

20.0

Models, Molecular

20.0

Genetic Markers

20.0

*Mutation, Missense

20.0