Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

A B C D E F G H I J K L M N O P Q R X Y Z



Gene Symbol
Gene NameAliasesPrevious_Symbol

COL11A2

collagen, type XI, alpha 2HKE5


Gene COL11A2 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Amino Acid Sequence

90.0

Animals

120.0

Collagen Type XI/*genetics

480.0

Mice

90.0

Molecular Sequence Data

130.0

Promoter Regions (Genetics)

20.0

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

350.0

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

180.0

Sequence Homology, Amino Acid

30.0

Abnormalities, Multiple/*genetics/pathology

45.0

Base Sequence

120.0

Child, Preschool

70.0

DNA Mutational Analysis

40.0

Face/abnormalities

34.0

Female

240.0

Humans

440.0

Male

250.0

Pedigree

170.0

Syndrome

130.0

Alleles

30.0

Heterozygote

20.0

Mice, Inbred C57BL

20.0

Collagen/*genetics

194.0

Comparative Study

30.0

Mice, Transgenic

20.0

Microscopy, Electron

20.0

Phenotype

40.0

Audiometry, Pure-Tone

25.0

Cross-Sectional Studies

30.0

Disease Progression

30.0

Genes, Dominant

30.0

Hearing Loss, Sensorineural/diagnosis/*genetics

212.0

*Linkage (Genetics)

60.0

Mutation

70.0

Adolescent

50.0

Adult

110.0

Aged

60.0

Child

60.0

Infant

40.0

Middle Aged

90.0

Alternative Splicing

20.0

Cells, Cultured

30.0

Exons

50.0

Introns

20.0

Linkage Disequilibrium

20.0

Spine/*pathology

250.0

Chromosome Mapping

90.0

Chromosomes, Human, Pair 6

42.0

Ossification of Posterior Longitudinal Ligament/*genetics

375.0

Cloning, Molecular

20.0

Japan

30.0

Linkage (Genetics)/genetics

31.0

Major Histocompatibility Complex/*genetics

53.0

Phylogeny

20.0

Analysis of Variance

20.0

Chromosome Disorders

20.0

Linear Models

20.0

DNA Primers

30.0

Polymerase Chain Reaction

20.0

Procollagen/*genetics

43.0

Exons/genetics

30.0

*Mutation

50.0

Mutation/*genetics

30.0

Connective Tissue Diseases/*genetics

337.0

Hearing Loss, Sensorineural/*genetics

22.0

Prevalence

20.0

DNA/genetics

20.0

Connective Tissue Diseases/*genetics/pathology

240.0

Ear/abnormalities

220.0

Eye Diseases, Hereditary/genetics/pathology

266.0

Joints/abnormalities

266.0

Gene Frequency

30.0

Haplotypes

30.0

Receptors, Retinoic Acid/*genetics

23.0

Retinoid X Receptors

20.0

Transcription Factors/*genetics

20.0

Variation (Genetics)

20.0

Eye Diseases/genetics

215.0

Sequence Analysis, DNA

20.0

Chromosomes, Human, Pair 19

21.0

Genetic Markers

20.0

Mutation/genetics

20.0

Polymorphism, Restriction Fragment Length

20.0

Collagen/genetics

22.0

Eye Diseases/*genetics

211.0

Linkage (Genetics)

30.0

Sequence Homology, Nucleic Acid

40.0

Genotype

20.0

*Chromosome Mapping

20.0

*Chromosomes, Human, Pair 6

51.0

Cosmids

30.0

DNA

20.0

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

20.0

Blotting, Southern

30.0

Restriction Mapping

20.0

Infant, Newborn

20.0