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Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

PHOX2A

paired-like (aristaless) homeobox 2aPMX2A, HGNC:3653, CFEOM2aristaless (Drosophila) homeobox, aristaless homeobox (Drosophila), fibrosis of extraocular muscles, congenital, 2, autosomal recessive


Gene PHOX2A gene interaction
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MeSH term
FrequencyCondition_Probility

Humans

190.0

5' Untranslated Regions/physiology

266.0

Animals

90.0

Binding Sites/physiology

21.0

Cell Differentiation

30.0

Mutagenesis, Site-Directed

20.0

Norepinephrine/*metabolism

25.0

Rats

60.0

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

150.0

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

140.0

Structure-Activity Relationship

30.0

Transfection

60.0

Cell Line

50.0

Genes, Reporter

50.0

Neuroblastoma/metabolism

23.0

Trans-Activation (Genetics)/physiology

22.0

Amino Acid Sequence

30.0

Base Sequence

70.0

Cloning, Molecular

20.0

DNA-Binding Proteins/physiology

20.0

Molecular Sequence Data

60.0

Nerve Tissue Proteins/genetics/*physiology

26.0

*Promoter Regions (Genetics)

20.0

*Trans-Activation (Genetics)

20.0

DNA Mutational Analysis

50.0

Female

80.0

Homeodomain Proteins/*genetics

40.0

Male

70.0

Pedigree

20.0

Phenotype

60.0

Reverse Transcriptase Polymerase Chain Reaction

20.0

Sequence Alignment

20.0

Transcription Factors/*genetics

40.0

Autonomic Nervous System/embryology/metabolism

266.0

DNA/metabolism

20.0

Hela Cells

20.0

Promoter Regions (Genetics)

30.0

Trans-Activation (Genetics)

20.0

Bone Morphogenetic Proteins/pharmacology

26.0

Cells, Cultured

30.0

Homeodomain Proteins/genetics

31.0

Transcription Factors/genetics

30.0

*Transforming Growth Factor beta

21.0

Genotype

20.0

Mice

50.0

Mice, Knockout

30.0

Norepinephrine/*physiology

213.0

*Mutation

20.0

Nerve Tissue Proteins/*genetics

20.0

Oculomotor Muscles/*pathology

240.0

Polymerase Chain Reaction

20.0

Homeodomain Proteins/*genetics/metabolism

22.0

Transcription Factors/*genetics/metabolism

20.0

Tumor Cells, Cultured

20.0

Promoter Regions (Genetics)/genetics

20.0

Dopamine beta-Hydroxylase/*genetics

24.0

In Situ Hybridization

20.0

Mutation

20.0

Pregnancy

20.0

Child

20.0

Child, Preschool

20.0

Infant

20.0

Syndrome

20.0