Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

NPHS1

nephrosis 1, congenital, Finnish type (nephrin)CNF, NPHN


Gene NPHS1 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Heterozygote

20.0

Humans

430.0

Mutation

120.0

Nephrotic Syndrome/*genetics

215.0

Proteins/*genetics

100.0

Proteinuria/*genetics

228.0

Alleles

30.0

Female

110.0

Finland

62.0

Genotype

70.0

Pregnancy

30.0

Proteins/*genetics/metabolism

20.0

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

340.0

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

140.0

Animals

180.0

Immunohistochemistry

30.0

Mice

120.0

RNA, Messenger/analysis

40.0

Base Sequence

60.0

Gene Expression Regulation

20.0

Molecular Sequence Data

90.0

Child, Preschool

30.0

Infant

50.0

Proteinuria/etiology

310.0

Gene Targeting

20.0

Proteins/genetics

50.0

Adult

60.0

Child

60.0

DNA Mutational Analysis

40.0

Glomerulosclerosis, Focal/genetics

360.0

Male

130.0

Phenotype

30.0

Membrane Proteins/metabolism

20.0

Phosphoproteins/metabolism

20.0

Biological Transport

20.0

Cell Line

60.0

Gene Expression

50.0

Microscopy, Fluorescence

40.0

Microscopy, Immunoelectron

30.0

Nephrotic Syndrome/congenital/genetics

375.0

Cell Membrane/metabolism

30.0

In Situ Hybridization

40.0

*Protein Biosynthesis

40.0

Protein Structure, Tertiary

30.0

Reverse Transcriptase Polymerase Chain Reaction

30.0

Tissue Distribution

20.0

Cells, Cultured

20.0

Comparative Study

40.0

Fluorescent Antibody Technique, Indirect

20.0

Kidney/cytology

31.0

Sensitivity and Specificity

20.0

Signal Transduction

30.0

Exons/genetics

20.0

Animals, Newborn

20.0

Blotting, Western

50.0

Genes, Reporter

20.0

Homozygote

20.0

Microscopy, Electron

30.0

Time Factors

20.0

Genes, Recessive

40.0

Infant, Newborn

30.0

*Mutation, Missense

30.0

Nephrotic Syndrome/congenital/*genetics

3100.0

Proteins/analysis/*genetics

26.0

Phosphorylation

30.0

Tyrosine/metabolism

20.0

Amino Acid Sequence

50.0

Blotting, Northern

20.0

Polymerase Chain Reaction

20.0

Rats

20.0

Rats, Sprague-Dawley

20.0

Cloning, Molecular

30.0

Glomerular Filtration Rate

21.0

Nephrotic Syndrome/genetics

233.0

Cosmids

20.0

Finland/epidemiology

21.0

Incidence

20.0

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

30.0

Aged

40.0

Gene Frequency

20.0

Middle Aged

50.0

Adolescent

30.0

Case-Control Studies

20.0

Genetic Markers

20.0

Species Specificity

20.0

Mice, Inbred C57BL

20.0

Mice, Mutant Strains

30.0

Membrane Proteins/*genetics/metabolism

21.0

Transfection

20.0

Proteins/*metabolism

20.0

Membrane Proteins/genetics

30.0