IthaID: 52
Names and Sequences
| Functionality: | Globin gene causative mutation | Pathogenicity: | Pathogenic / Likely Pathogenic |
|---|---|---|---|
| Common Name: | CD 3 (+T) | HGVS Name: | HBB:c.11dupT |
| Hb Name: | N/A | Protein Info: | N/A |
Context nucleotide sequence:
ACCTCAAACAGACACCATGGTGCATCT [-/T] GACTCCTGAGGAGAAGTCTGCCGTTA (Strand: -)
Also known as:
Comments: Found in three chromosomes among Turkish patients from Antalya. The insertion of a nt T in codon 3 creates a shift in the reading frame with a premature stop codon at codon 6 (TGA).
We follow the HGVS sequence variant nomenclature and IUPAC standards.
External Links
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: | 70605 |
| Size: | 1 bp |
| Located at: | β |
| Specific Location: | Exon 1 |
Other details
| Type of Mutation: | Point-Mutation(Insertion) |
|---|---|
| Effect on Gene/Protein Function: | Frameshift (Translation) |
| Ethnic Origin: | Turkish |
| Molecular mechanism: | N/A |
| Inheritance: | Recessive |
| DNA Sequence Determined: | No |
In silico pathogenicity prediction
Note:
The impact thresholds provided in this section are based on the analyses performed in Tamana et.al. For any given tool, the impact thresholds defined for the set of variants with the same effect on function as the variant examined, are preferred over those defined for the full dataset.
Sequence Viewer
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Publications / Origin
- Keser I, Sanlioglu AD, Manguoglu E, Guzeloglu Kayisli O, Nal N, Sargin F, Yesilipek A, Simsek M, Mendilcioglu I, Canatan D, Luleci G, Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya., Acta haematologica, 111(4), 205-10, 2004 PubMed
Created on 2010-06-16 16:13:14,
Last reviewed on 2019-11-13 16:09:12 (Show full history)
| A/A | Date | Curator(s) | Comments |
|---|---|---|---|
| 1 | 2010-06-16 16:13:14 | The IthaGenes Curation Team | Created |
| 2 | 2013-10-15 17:28:32 | The IthaGenes Curation Team | Reviewed. |
| 3 | 2019-11-13 16:09:12 | The IthaGenes Curation Team | Reviewed. Mutation names and Location corrected. Allele, Context sequence and Comment added. |
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IthaGenes was last updated on 2024-11-20 13:24:07