Pubdiz
Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

HOXD13

homeo box D13


Gene HOXD13 gene interaction
View Neighborhood Gene

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

MeSH term
FrequencyCondition_Probility

Humans

330.0

Alanine/genetics

21.0

Base Sequence

120.0

DNA/chemistry/genetics

20.0

DNA Mutational Analysis

70.0

Family Health

20.0

Female

180.0

Genotype

20.0

Homeodomain Proteins/*genetics

102.0

Male

230.0

Molecular Sequence Data

150.0

Pedigree

130.0

Peptides/genetics

22.0

Polydactyly/*genetics/pathology

266.0

Polymorphism, Genetic

20.0

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

270.0

Syndactyly/*genetics/pathology

3100.0

*Transcription Factors

181.0

Trinucleotide Repeat Expansion/*genetics

23.0

Alleles

20.0

Exons/genetics

20.0

Peptides/*genetics

33.0

Syndrome

50.0

Animals

140.0

*Genes, Homeobox

52.0

Mice

90.0

Polymerase Chain Reaction

40.0

Sequence Alignment

30.0

Homeodomain Proteins/genetics/*metabolism

32.0

Mutation

70.0

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

70.0

Sequence Deletion

30.0

Adolescent

20.0

Amino Acid Sequence

50.0

Blotting, Southern

20.0

*Chromosomes, Human, Pair 11

20.0

*Chromosomes, Human, Pair 2

31.0

Gene Expression Regulation, Leukemic

22.0

Gene Fusion

22.0

Homeodomain Proteins/biosynthesis/*genetics

29.0

RNA, Messenger/genetics

20.0

Reverse Transcriptase Polymerase Chain Reaction

20.0

Phenotype

80.0

Transcription, Genetic

20.0

Adult

20.0

Child, Preschool

30.0

Chromosomes, Human, Pair 2/*genetics

21.0

In Situ Hybridization, Fluorescence

30.0

Infant, Newborn

30.0

Karyotyping

30.0

Mutation/*genetics

20.0

Body Patterning

23.0

Homeodomain Proteins/*genetics/metabolism

22.0

Homozygote

30.0

Mice, Mutant Strains

20.0

Homeodomain Proteins/genetics

62.0

Polydactyly/*genetics

418.0

Syndactyly/*genetics

538.0

Gene Expression Regulation, Developmental

20.0

Child

30.0

English Abstract

20.0

Cell Transformation, Neoplastic/genetics

20.0

*Nuclear Pore Complex Proteins

22.0

*Translocation, Genetic

20.0

Chromosomes, Human, Pair 2

31.0

Gene Deletion

30.0

Genetic Markers

20.0

Multigene Family

40.0

Fingers/*abnormalities

323.0

Linkage (Genetics)

20.0

Lod Score

20.0

Toes/*abnormalities

327.0

Chromosome Mapping

50.0

Heterozygote

30.0

*Mutation

20.0

In Situ Hybridization

20.0

Transcription Factors/genetics

30.0

Morphogenesis

20.0

Haplotypes

20.0

Hand Deformities, Congenital/*genetics

212.0

Limb Deformities, Congenital/*genetics

315.0

Polydactyly/genetics

29.0

Syndactyly/genetics

222.0