IthaID: 148
Names and Sequences
| Functionality: | Globin gene causative mutation | Pathogenicity: | Pathogenic / Likely Pathogenic |
|---|---|---|---|
| Common Name: | CD 42/43 (+T) | HGVS Name: | HBB:c.129dupT |
| Hb Name: | N/A | Protein Info: | N/A |
Context nucleotide sequence:
CTACCCTTGGACCCAGAGGTTCTTT [-/T] GAGTCCTTTGGGGATCTGTCCACTC (Strand: -)
Also known as:
We follow the HGVS sequence variant nomenclature and IUPAC standards.
Phenotype
| Hemoglobinopathy Group: | Thalassaemia |
|---|---|
| Hemoglobinopathy Subgroup: | β-thalassaemia |
| Allele Phenotype: | β0 |
| Associated Phenotypes: |
Haemolytic anaemia [HP:0001878] Ineffective erythropoiesis [HP:0010972] |
Location
| Chromosome: | 11 |
|---|---|
| Locus: | NG_000007.3 |
| Locus Location: | 70853 |
| Size: | 1 bp |
| Located at: | β |
| Specific Location: | Exon 2 |
Other details
| Type of Mutation: | Point-Mutation(Insertion) |
|---|---|
| Effect on Gene/Protein Function: | Frameshift (Translation) |
| Ethnic Origin: | Japanese |
| Molecular mechanism: | N/A |
| Inheritance: | Recessive |
| DNA Sequence Determined: | No |
In silico pathogenicity prediction
Frequencies
Publications / Origin
- Oshima K, Harano T, Harano K, Japanese beta zero-thalassemia: molecular characterization of a novel insertion causing a stop codon., American journal of hematology, 52(1), 39-41, 1996
Created on 2010-06-16 16:13:15,
Last reviewed on 2019-11-13 12:26:39 (Show full history)
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