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Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

EDNRB

endothelin receptor type BETB, HGNC:5207


Gene EDNRB gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Chromosome Mapping

90.0

*Chromosomes, Human, Pair 1

20.0

Female

330.0

Genetic Predisposition to Disease

30.0

Humans

770.0

Male

360.0

Pedigree

150.0

Recurrence

20.0

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

470.0

Animals

320.0

Child

110.0

*Drosophila Proteins

161.0

Endothelin-3/genetics

1292.0

Hirschsprung Disease/complications/*genetics

266.0

Infant

140.0

Mice

150.0

Mice, Knockout

20.0

*Mutation

210.0

Nerve Growth Factors/genetics

412.0

Proto-Oncogene Proteins/*genetics

101.0

Receptor Protein-Tyrosine Kinases/*genetics

123.0

Receptor, Endothelin B

4270.0

Receptors, Endothelin/genetics

1386.0

Alleles

30.0

Chromosomes, Human, Pair 10/genetics

22.0

Genetic Markers

30.0

Hirschsprung Disease/*genetics

3445.0

Models, Genetic

20.0

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

160.0

Base Sequence

180.0

*DNA Methylation

71.0

DNA Primers/chemistry

30.0

Gene Expression

40.0

Molecular Sequence Data

200.0

Promoter Regions (Genetics)/*genetics

20.0

Receptors, Endothelin/*genetics/metabolism

7100.0

Reverse Transcriptase Polymerase Chain Reaction

60.0

Tumor Cells, Cultured

70.0

Consanguinity

30.0

DNA Mutational Analysis

80.0

DNA-Binding Proteins/genetics

30.0

Homozygote

50.0

Mutation

140.0

Phenotype

120.0

Receptors, Endothelin/*genetics

2488.0

Syndrome

40.0

Waardenburg's Syndrome/genetics

314.0

Disease Models, Animal

30.0

Hirschsprung Disease/*genetics/pathology

228.0

Mice, Inbred Strains

20.0

Exons/genetics

20.0

Polymerase Chain Reaction/methods

20.0

Cell Line

30.0

Mice, Inbred C57BL

40.0

Pregnancy

20.0

*Chromosome Deletion

20.0

Comparative Study

70.0

Karyotyping

20.0

Nucleic Acid Hybridization

20.0

Amino Acid Sequence

100.0

CHO Cells

30.0

Calcium/metabolism

40.0

Hamsters

30.0

Protein Binding

40.0

Sequence Homology, Amino Acid

50.0

Signal Transduction

60.0

Transfection

30.0

Chromosomes, Human, Pair 1/genetics

21.0

Chromosomes, Human, Pair 13/genetics

34.0

DNA/genetics

30.0

Lod Score

20.0

English Abstract

70.0

CpG Islands/*genetics

22.0

*Promoter Regions (Genetics)

20.0

Prostatic Neoplasms/*genetics/metabolism

25.0

Case-Control Studies

40.0

Mutation/*genetics

20.0

*Nerve Growth Factors

42.0

Nerve Tissue Proteins/genetics

31.0

Polymorphism, Single-Stranded Conformational

100.0

Proto-Oncogene Proteins/genetics

50.0

Receptor Protein-Tyrosine Kinases/genetics

74.0

Sequence Analysis, DNA

50.0

Crosses, Genetic

20.0

Genes, Dominant

20.0

Mice, Inbred C3H

20.0

Cloning, Molecular

40.0

Hair Color/*genetics

27.0

Linkage (Genetics)/*genetics

20.0

Sequence Alignment

20.0

Aged

40.0

Glutathione Transferase/genetics

20.0

Isoenzymes/genetics

20.0

Middle Aged

50.0

Polymerase Chain Reaction

60.0

Prognosis

20.0

Promoter Regions (Genetics)

30.0

Receptors, Retinoic Acid/genetics

22.0

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

20.0

Tumor Suppressor Proteins/genetics

34.0

Adult

40.0

Chromosomes, Human, Pair 10

21.0

Point Mutation

40.0

COS Cells

20.0

DNA Primers

20.0

Endothelin-1/metabolism

210.0

Endothelin-3/metabolism

2100.0

Ligands

20.0

In Situ Hybridization

30.0

Trans-Activation (Genetics)

20.0

Amino Acid Substitution

30.0

Child, Preschool

90.0

Infant, Newborn

70.0

Variation (Genetics)

40.0

Endothelin-3/*genetics

583.0

Nerve Tissue Proteins/*genetics

30.0

Polymorphism, Genetic

20.0

Sensitivity and Specificity

30.0

Sequence Deletion

20.0

DNA-Binding Proteins/*genetics

30.0

Epistasis, Genetic

23.0

Transcription Factors/genetics

20.0

Waardenburg's Syndrome/*genetics

25.0

Family Health

20.0

Adolescent

40.0

RNA, Messenger/genetics

20.0

*Point Mutation

30.0

Blotting, Northern

20.0

Gene Deletion

40.0

RNA, Messenger/analysis

20.0

Heterozygote

90.0

Gene Expression Regulation, Neoplastic

20.0

Open Reading Frames

20.0

Sequence Homology, Nucleic Acid

20.0

Tissue Distribution

30.0

Transcription, Genetic

30.0

Cell Differentiation

20.0

Cell Division

20.0

Cells, Cultured

20.0

RNA, Messenger

20.0

Melanocytes

240.0

Rats

40.0

DNA, Complementary

20.0

Horse Diseases/*genetics

240.0

Exons

40.0

Disease Progression

20.0

*Gene Silencing

21.0

Hirschsprung Disease/genetics

318.0

Neuroblastoma/*genetics

22.0

Haplotypes

20.0

Genotype

40.0

Germ-Line Mutation

20.0

Neural Crest/growth & development

266.0

Hirschsprung Disease/*genetics/physiopathology

3100.0

Chromosomes, Human, Pair 13

21.0

Linkage Disequilibrium

30.0

China

20.0

Receptor, Endothelin B/*genetics

2100.0

Polymorphism, Single Nucleotide

20.0

Transcription Factors/*genetics

20.0

Proto-Oncogene Proteins/*genetics/metabolism

21.0

Receptor Protein-Tyrosine Kinases/*genetics/metabolism

23.0

High Mobility Group Proteins/*genetics

22.0