IthaID: 1513
Names and Sequences
Functionality: | Globin gene causative mutation | Pathogenicity: | N/A |
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Common Name: | Thai/Vietnamese (δβ)0 | HGVS Name: | NG_000007.3:g.64384_76993del |
Hb Name: | N/A | Protein Info: | N/A |
Also known as: Thai (δβ)0 , Vietnamese (δβ)0
Comments: The Thai/Vietnamese (δβ)0 thalassaemia deletion is commonly found in Southeast Asia with variable descriptions in literature. It was first reported as Thai (δβ)0-thalassaemia with a deletion size of approximately 12.5 kb and breakpoints localised by restriction endonuclease mapping. The proband was a Thai female presenting with mild anaemia, normal HbA2 and elevated HbF at 9.9% [PMID: 2454901]. It was later confirmed by simple gap-PCR and reported by several groups across Thailand. Breakpoint sequencing analysis localised the 5’ breakpoint between 35432-35620 in the IVS-II of the δ-globin gene and the 3’ breakpoint at 23090 within the L1 repeat sequence at 4.7 kb 3’ of the β-globin gene (NCBI_AC104389.8 coordinates) [PMID: 23181748]. Another study identified the Thai (δβ)0 deletion in two Thai families and reported breakpoint coordinates 55990-68575 (GenBank HUMBB) with a deletion size of 12.585 kb [PMID: 11860449]. On a similar note, the Vietnamese (δβ)0 thalassaemia deletion extends from the IVS-II of the δ-globin gene to the L1 repeat sequence 3’ of the β-globin gene. It has a stated deletion size of 12.585 kb with coordinate numbers 56007-68591 or 56008-68592 (Genbank HUMBB) due to the presence of a single base (T) homology common to both ends [PMID: 7510147]. In spite of differences in the reported coordinate numbers, the breakpoint sequences for the Thai (δβ)0 and Vietnamese (δβ)0 deletions are identical. Another study reported a 12.61 kb deletion with similar breakpoints extending from 5241853-5254462 (GRCh37.p5, NC_000011.9 co-ordinates) in a patient from India with elevated HbF at 21.3% [PMID: 22801970]. Further analysis showed that this deletion is in fact the same as the Thai/Vietnamese (δβ)0 deletion [PMID: 24006412]. The deletion size based on the breakpoint sequence information provided in these papers was determined to be 12.610 kb (GRCh38.p12, NC_000011.10). Furthermore, the Thai/Vietnamese (δβ)0 deletion is reported to be similar to the Laotian (δβ)0 deletion [ithaID=1512], with stated 5′ breakpoint between 775-781 in IVS-II of the δ-globin gene and 3′ breakpoint laying 4.7 kb downstream of the β-globin gene [PMID: 2458154]. In the absence of breakpoint sequence information for the latter and given that the breakpoints lie in regions with propensity for higher recombination rate (AT-rich region-Alu and the L1 repeats), there exists a possibility that the Laotian (δβ)0 and Thai/Vietnamese (δβ)0 deletions are not the same.
We follow the HGVS sequence variant nomenclature and IUPAC standards.
External Links
Phenotype
Hemoglobinopathy Group: | Thalassaemia |
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Hemoglobinopathy Subgroup: | δβ-thalassaemia |
Allele Phenotype: | GγAγ(δβ)0 |
Associated Phenotypes: | Haemolytic anaemia [HP:0001878] |
Location
Chromosome: | 11 |
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Locus: | NG_000007.3 |
Locus Location: | 64384 |
Size: | 12.61 kb |
Deletion involves: | δ, β |
Other details
Type of Mutation: | Deletion |
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Ethnic Origin: | Thai, Vietnamese, Indian |
Molecular mechanism: | N/A |
Inheritance: | Recessive |
DNA Breakpoint Determined: | Yes |
In silico pathogenicity prediction
Publications / Origin
- Zhang JW, Stamatoyannopoulos G, Anagnou NP, Laotian (delta beta) (0)-thalassemia: molecular characterization of a novel deletion associated with increased production of fetal hemoglobin., Blood, 72(3), 983-8, 1988
- Trent RJ, Svirklys L, Jones P, Thai (delta beta)0-thalassemia and its interaction with gamma-thalassemia., Hemoglobin, 12(2), 101-14, 1988
- Craig JE, Barnetson RA, Prior J, Raven JL, Thein SL, Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification., Blood, 83(6), 1673-82, 1994
- Fucharoen S, Pengjam Y, Surapot S, Fucharoen G, Sanchaisuriya K, Molecular characterization of (deltabeta)(0)/beta(0)-thalassemia and (deltabeta)(0)-thalassemia/hemoglobin E in Thai patients., Eur. J. Haematol., 67(4), 258-62, 2001
- Tritipsombut J, Phylipsen M, Viprakasit V, Chalaow N, Sanchaisuriya K, Giordano PC, Fucharoen S, Harteveld CL, A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast Asia., Hemoglobin, 36(6), 571-80, 2012
- Ghedira ES, Lecerf L, Faubert E, Costes B, Moradkhani K, Bachir D, Galactéros F, Pissard S, Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region., Haematologica, 98(2), 305-8, 2013
A/A | Date | Curator(s) | Comments |
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1 | 2010-06-16 16:13:17 | The IthaGenes Curation Team | Created |
2 | 2013-10-15 17:28:32 | The IthaGenes Curation Team | Reviewed. |
3 | 2020-01-03 14:05:13 | The IthaGenes Curation Team | Reviewed. Common name changed and Synonym names added. References, Comment and Ethnic origin added. |
4 | 2020-01-03 14:23:22 | The IthaGenes Curation Team | Reviewed. Chromosomal location added. |
5 | 2020-01-03 14:25:16 | The IthaGenes Curation Team | Reviewed. Phenotype added. |
6 | 2020-01-03 14:32:49 | The IthaGenes Curation Team | Reviewed. HGVS name added |
7 | 2020-01-03 14:36:20 | The IthaGenes Curation Team | Reviewed. Edits. |
8 | 2020-01-03 14:43:19 | The IthaGenes Curation Team | Reviewed. Deletion size and coordinates corrected based on sequence info. |
9 | 2020-01-07 09:04:45 | The IthaGenes Curation Team | Reviewed. HGVS name corrected. |
10 | 2020-01-07 11:55:09 | The IthaGenes Curation Team | Reviewed. |