Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

FOXL2

forkhead box L2BPES1


Gene FOXL2 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Aged

30.0

Humans

190.0

Base Sequence

90.0

DNA-Binding Proteins/*genetics

120.0

Eyelid Diseases/*genetics

2100.0

Female

200.0

Male

130.0

*Mutation

50.0

Pedigree

90.0

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

180.0

Transcription Factors/*genetics

120.0

Blepharophimosis/*genetics

666.0

Blepharoptosis/*genetics

333.0

Syndrome

110.0

Adult

50.0

Amino Acid Sequence

90.0

Child, Preschool

30.0

Eyelids/*abnormalities

466.0

Genes, Dominant

30.0

Molecular Sequence Data

120.0

*Sequence Deletion

30.0

Animals

130.0

Open Reading Frames

20.0

Transcription Factors/genetics

30.0

Gene Deletion

20.0

Models, Genetic

20.0

Mutation, Missense

20.0

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

40.0

Blepharophimosis/genetics

240.0

Blepharoptosis/genetics

233.0

Child

30.0

DNA-Binding Proteins/genetics

20.0

Gene Duplication

21.0

Mice

100.0

Sequence Homology, Amino Acid

20.0

Comparative Study

40.0

Sequence Alignment

30.0

Transcription Factors/genetics/metabolism

20.0

Conserved Sequence

30.0

Conserved Sequence/genetics

31.0

Goats/genetics

250.0

RNA, Messenger/genetics/metabolism

20.0

Eyelids/abnormalities

360.0

DNA Mutational Analysis

20.0

Middle Aged

20.0

Mutation

50.0

Transcription, Genetic

20.0

Abnormalities, Multiple/genetics

22.0