IthaID: 1522



Names and Sequences

Functionality: Globin gene causative mutation Pathogenicity: N/A
Common Name: Malaysian-1 (Aγδβ)0 HGVS Name: N/A
Hb Name: N/A Protein Info: N/A

Also known as:

We follow the HGVS sequence variant nomenclature and IUPAC standards.

External Links

Phenotype

Hemoglobinopathy Group: Thalassaemia
Hemoglobinopathy Subgroup: δβ-thalassaemia
Allele Phenotype:Gγ(Aγδβ)0
Associated Phenotypes: N/A

Location

Chromosome: 11
Locus: NG_000007.3
Locus Location: N/A
Size: N/A
Deletion involves: , δ, β, pseudo β

Other details

Type of Mutation: Deletion
Ethnic Origin: Malay
Molecular mechanism: N/A
Inheritance: Recessive
DNA Breakpoint Determined: No

In silico pathogenicity prediction

Sequence Viewer

Note: The NCBI Sequence Viewer is not installed on the ITHANET servers but it is embedded in this page from the NCBI. Therefore, IthaGenes has no responsibility over any temporary unavailability of the service. In such a case, please Refresh the page or retry at a later stage. Otherwise, use this external link.

Publications / Origin

  1. Trent RJ, Jones RW, Clegg JB, Weatherall DJ, Davidson R, Wood WG, (A gamma delta beta) thalassaemia: similarity of phenotype in four different molecular defects, including one newly described., British journal of haematology, 57(2), 279-89, 1984 PubMed
Created on 2010-06-16 16:13:17, Last reviewed on 2014-06-04 10:34:51 (Show full history)

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