Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

GLRA1

glycine receptor, alpha 1 (startle disease/hyperekplexia, stiff man syndrome)


Gene GLRA1 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Base Sequence

100.0

Cell Line

30.0

Child

30.0

DNA/metabolism

20.0

DNA Mutational Analysis

50.0

Electrophysiology

40.0

Exons

30.0

Family Health

20.0

Female

140.0

Humans

270.0

Male

130.0

Molecular Sequence Data

120.0

*Mutation

30.0

Pedigree

80.0

Point Mutation

30.0

Receptors, Glycine/*genetics

1684.0

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

210.0

Startle Reaction/*genetics

990.0

Child, Preschool

20.0

Infant

30.0

Infant, Newborn

50.0

Nervous System Diseases/*genetics

516.0

Sequence Analysis, DNA

20.0

Amino Acid Sequence

90.0

Binding Sites/genetics

20.0

Mutation, Missense

20.0

Sequence Homology, Amino Acid

30.0

Startle Reaction/genetics

350.0

DNA, Complementary/genetics

20.0

Heterozygote

20.0

Polymorphism, Single-Stranded Conformational

20.0

Reflex, Abnormal/*genetics

3100.0

Alleles

30.0

Blotting, Western

20.0

Kinetics

20.0

Models, Chemical

20.0

Mutation

70.0

Protein Binding

20.0

Protein Structure, Tertiary

20.0

Muscle Rigidity/*genetics

2100.0

Startle Reaction/*physiology

360.0

Chromosome Mapping

40.0

Comparative Study

30.0

In Situ Hybridization, Fluorescence

20.0

Acoustic Stimulation

22.0

Animals

60.0

Mice

40.0

Mice, Neurologic Mutants

21.0

Polymerase Chain Reaction

20.0

Linkage (Genetics)

20.0

Adolescent

40.0

Adult

40.0

*Startle Reaction

2100.0

Genes, Recessive

20.0

Receptors, Glycine/chemistry/*genetics

2100.0

Polymorphism, Genetic

20.0

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

30.0

Clonazepam/therapeutic use

240.0

Receptors, Glycine/genetics

250.0

*Chromosomes, Human, Pair 5

20.0

*Point Mutation

20.0

Point Mutation/*genetics

20.0

Receptors, Glycine/genetics/*metabolism

2100.0

Syndrome

20.0