Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

CLN5

ceroid-lipofuscinosis, neuronal 5


Gene CLN5 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Animals

90.0

Base Sequence

50.0

Humans

390.0

Mice

40.0

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

280.0

Sequence Deletion

20.0

Adolescent

120.0

Adult

100.0

Child

170.0

Female

140.0

Male

120.0

Membrane Proteins/genetics

51.0

Age of Onset

50.0

Genotype

60.0

Phenotype

70.0

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

90.0

Child, Preschool

140.0

Infant

100.0

Infant, Newborn

20.0

Finland

41.0

Mutation

70.0

Chromosome Mapping

70.0

Neuronal Ceroid-Lipofuscinosis/*genetics

1220.0

DNA Mutational Analysis

40.0

Homozygote

20.0

Magnetic Resonance Imaging

20.0

Membrane Proteins/*genetics

40.0

Neuronal Ceroid-Lipofuscinosis/diagnosis/epidemiology/*genetics

266.0

Microscopy, Electron

20.0

Amino Acid Sequence

20.0

COS Cells

20.0

Molecular Sequence Data

40.0

Hydrogen-Ion Concentration

20.0

*Membrane Glycoproteins

30.0

*Molecular Chaperones

32.0

Polymorphism, Genetic

40.0

Incidence

20.0

Linkage (Genetics)

40.0

Gene Deletion

20.0

Haplotypes

30.0

Pregnancy

30.0

*Prenatal Diagnosis

20.0

Neuronal Ceroid-Lipofuscinosis/classification/*genetics

250.0

Microsatellite Repeats

30.0

Pedigree

70.0

*Chromosomes, Human, Pair 13

42.0

*Mutation

50.0

Tissue Distribution

20.0

Transcription Factors/*genetics

20.0

Genetic Markers

50.0

Lod Score

20.0

*Chromosome Mapping

20.0

Chromosomes, Human, Pair 13

21.0

Genetic Markers/genetics

20.0

Membrane Glycoproteins/genetics

21.0

Molecular Chaperones/genetics

29.0

Neuronal Ceroid-Lipofuscinosis/diagnosis/*genetics/pathology

375.0

*Variation (Genetics)

20.0

Polymerase Chain Reaction

20.0

Recombination, Genetic

20.0

*Linkage Disequilibrium

21.0

*Chromosomes, Human, Pair 1

20.0

*Chromosomes, Human, Pair 16

31.0

Alleles

20.0

Lysosomes/metabolism

21.0