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Taipei Medical University

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Gene Symbol
Gene NameAliasesPrevious_Symbol

ALAS2

aminolevulinate, delta-, synthase 2 (sideroblastic/hypochromic anemia)


Gene ALAS2 gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Animals

150.0

Genetic Vectors

20.0

Hamsters

20.0

Hela Cells

30.0

Humans

480.0

RNA, Messenger/metabolism

20.0

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

330.0

*Transcription, Genetic

20.0

Transfection

20.0

5-Aminolevulinate Synthetase/*genetics

2388.0

Adult

110.0

Anemia, Sideroblastic/*genetics

1368.0

Codon, Nonsense

32.0

Male

270.0

Mutation, Missense

30.0

Aged

60.0

Aged, 80 and over

40.0

Codon

20.0

Female

240.0

Family Health

70.0

Base Sequence

150.0

DNA Mutational Analysis

30.0

Linkage (Genetics)

100.0

Middle Aged

60.0

Mutation

70.0

X Chromosome/*genetics

82.0

Adolescent

50.0

Alleles

20.0

Blood Transfusion

21.0

Heterozygote

30.0

Pedigree

130.0

Pyridoxine/therapeutic use

428.0

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

230.0

Conserved Sequence

20.0

Erythrocytes/*enzymology

81.0

Mice

50.0

Molecular Sequence Data

160.0

Mutagenesis, Site-Directed

30.0

Regulatory Sequences, Nucleic Acid

20.0

Sequence Analysis, DNA

20.0

Transcription, Genetic

20.0

Tumor Cells, Cultured

20.0

Chromosome Mapping

100.0

Genetic Markers

40.0

Hybrid Cells

30.0

Microsatellite Repeats

40.0

*X Chromosome

151.0

*Gene Expression Regulation, Enzymologic

20.0

Introns

20.0

Iron/metabolism

21.0

Transcription Factors/metabolism

40.0

5-Aminolevulinate Synthetase/blood/*genetics

2100.0

Exons

30.0

*Mutation, Missense

20.0

Polymerase Chain Reaction

70.0

Pyridoxine/*therapeutic use

220.0

Comparative Study

30.0

Centromere/genetics

22.0

Lod Score

40.0

Mental Retardation/*genetics

31.0

Polymorphism, Restriction Fragment Length

20.0

Syndrome

20.0

Child

30.0

DNA Primers

20.0

*Mutation

50.0

Haplotypes

20.0

Models, Genetic

30.0

Polymorphism, Genetic

30.0

Recombination, Genetic

30.0

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

30.0

Anemia, Sideroblastic/drug therapy/enzymology/*genetics

3100.0

Amino Acid Sequence

60.0

Cloning, Molecular

20.0

Phenotype

30.0

Sequence Homology, Amino Acid

30.0

Arginine/genetics

21.0

Point Mutation

40.0

5-Aminolevulinate Synthetase/*genetics/metabolism

2100.0

Genes, Reporter

30.0

Promoter Regions (Genetics)

20.0

5-Aminolevulinate Synthetase/genetics

360.0

Isoenzymes/genetics

20.0

*Linkage (Genetics)

40.0

Heme/biosynthesis

211.0

Binding Sites

20.0

Centromere

22.0

In Situ Hybridization

20.0

Mice, Inbred C57BL

20.0

Karyotyping

20.0

Oligonucleotide Probes

20.0

5-Aminolevulinate Synthetase/biosynthesis/*genetics

2100.0

*Point Mutation

20.0

Recombinant Fusion Proteins/biosynthesis

20.0

Mitochondria/metabolism

20.0

RNA, Messenger/biosynthesis

20.0