IthaID: 604
Names and Sequences
| Functionality: | Globin gene causative mutation | Pathogenicity: | Benign / Likely Benign |
|---|---|---|---|
| Common Name: | CD 72 CAC>CGC [His>Arg] | HGVS Name: | HBA2:c.218A>G |
| Hb Name: | Hb Daneshgah-Tehran | Protein Info: | α2 72(EF1) His>Arg |
Context nucleotide sequence:
GACGCGCTGACCAACGCCGTGGCGC [A/G] CGTGGACGACATGCCCAACGCGCTG (Strand: +)
Protein sequence:
MVLSPADKTNVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHGKKVADALTNAVARVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTPAVHASLDKFLASVSTVLTSKYR
Also known as:
We follow the HGVS sequence variant nomenclature and IUPAC standards.
Phenotype
| Hemoglobinopathy Group: | Structural Haemoglobinopathy |
|---|---|
| Hemoglobinopathy Subgroup: | α-chain variant |
| Allele Phenotype: | N/A |
| Stability: | N/A |
| Oxygen Affinity: | N/A |
| Associated Phenotypes: | N/A |
Location
| Chromosome: | 16 |
|---|---|
| Locus: | NG_000006.1 |
| Locus Location: | 34110 |
| Size: | 1 bp |
| Located at: | α2 |
| Specific Location: | Exon 2 |
Other details
| Type of Mutation: | Point-Mutation(Substitution) |
|---|---|
| Effect on Gene/Protein Function: | Missense codons (Protein Structure) |
| Ethnic Origin: | Argentine, Iranian |
| Molecular mechanism: | N/A |
| Inheritance: | Recessive |
| DNA Sequence Determined: | Yes |
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
- Rahbar S, Nowazari G, Danéshmand P, Haemoglobin Daneshgah-Tehran alpha2 72 (EPI) histidine--arginine betaA2., Nature New Biol. , 245(148), 268-9, 1973 PubMed
- de Weinstein BI, Kutlar A, Webber BB, Wilson JB, Huisman TH, Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family., Hemoglobin , 9(4), 409-11, 1985 PubMed
- Jorge SB, Melo MB, Costa FF, Sonati MF, Screening for mutations in human alpha-globin genes by nonradioactive single-strand conformation polymorphism., Braz. J. Med. Biol. Res. , 36(11), 1471-4, 2003 PubMed
Created on 2010-06-16 16:13:16,
Last reviewed on 2021-04-07 11:46:47 (Show full history)
| A/A | Date | Curator(s) | Comments |
|---|---|---|---|
| 1 | 2010-06-16 16:13:16 | The IthaGenes Curation Team | Created |
| 2 | 2013-10-15 17:00:14 | The IthaGenes Curation Team | Reviewed. |
| 3 | 2014-04-10 09:20:42 | The IthaGenes Curation Team | Reviewed. |
| 4 | 2021-04-07 11:46:47 | The IthaGenes Curation Team | Reviewed. HGVS, protein name and Locus location corrected. Reference added. |
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IthaGenes was last updated on 2024-11-20 13:24:07