Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

FOXC1

forkhead box C1FREAC3, ARA, IGDA, IHG1


Gene FOXC1 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Animals

180.0

Humans

310.0

Base Sequence

60.0

*Chromosome Deletion

20.0

Chromosomes, Human, Pair 6/*genetics

21.0

Cornea/*abnormalities

266.0

*DNA-Binding Proteins

150.0

Eye Abnormalities/*genetics

717.0

Female

160.0

Genotype

60.0

Glaucoma/*genetics

531.0

Iris/*abnormalities

750.0

Male

120.0

Microscopy, Fluorescence

20.0

Molecular Sequence Data

90.0

Pedigree

90.0

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

260.0

Transcription Factors/genetics

30.0

Abnormalities, Multiple/*genetics

20.0

Homeodomain Proteins/genetics

41.0

Mice

80.0

*Nuclear Proteins

30.0

Chromosomes, Human, Pair 4/genetics

22.0

Chromosomes, Human, Pair 6/genetics

21.0

DNA Mutational Analysis

70.0

DNA Primers/chemistry

20.0

Eye Abnormalities/ethnology/*genetics

2100.0

Homeodomain Proteins/*genetics

20.0

Mutation

50.0

Syndrome

70.0

Transcription Factors/*genetics

110.0

Amino Acid Sequence

70.0

COS Cells

40.0

DNA/metabolism

20.0

Fluorescent Antibody Technique, Indirect

30.0

Hela Cells

50.0

Mutagenesis

20.0

Phenotype

80.0

Protein Structure, Tertiary

30.0

Sequence Homology, Amino Acid

30.0

Trans-Activation (Genetics)

50.0

Adolescent

40.0

Anterior Eye Segment/*abnormalities

640.0

Child

40.0

Infant

50.0

Intraocular Pressure

27.0

*Mutation

20.0

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

100.0

Gene Expression

20.0

Rats

20.0

Aged

30.0

Middle Aged

40.0

Reverse Transcriptase Polymerase Chain Reaction

20.0

Cell Nucleus/chemistry

21.0

Models, Molecular

40.0

Protein Structure, Secondary

30.0

*Mutation, Missense

30.0

Protein Conformation

20.0

Sequence Alignment

20.0

Transcription Factors/*chemistry/*genetics/metabolism

225.0

Anterior Chamber/*abnormalities

240.0

Cercopithecus aethiops

30.0

Child, Preschool

20.0

Electrophoretic Mobility Shift Assay

20.0

Mutation, Missense

20.0

Plasmids

20.0

DNA-Binding Proteins/*genetics/physiology

33.0

Glaucoma/genetics

222.0

Haplotypes

20.0

Heterozygote

20.0

In Situ Hybridization

20.0

Intraocular Pressure/genetics

375.0

Mice, Mutant Strains

30.0

Transcription Factors/*genetics/physiology

44.0

Gene Expression Regulation, Developmental

30.0

Mice, Knockout

20.0

Mice, Transgenic

30.0

Models, Biological

30.0

Pregnancy

20.0

Microsatellite Repeats

20.0

DNA-Binding Proteins/*genetics

30.0

Sequence Analysis, DNA

20.0

Adult

70.0

Polymerase Chain Reaction

40.0

Eye Abnormalities/genetics

27.0

Anterior Eye Segment/*abnormalities/pathology

2100.0

Disease Models, Animal

20.0

*Gene Expression Regulation

20.0

Infant, Newborn

20.0