IthaID: 3973
Names and Sequences
Functionality: | Globin gene causative mutation | Pathogenicity: | N/A |
---|---|---|---|
Common Name: | -α3.7;CD 68 AAC>AAR | HGVS Name: | NG_000006.1:g.[34099C>R;34247_38050del] |
Hb Name: | Hb G-Philadelphia | Protein Info: | N/A |
Also known as: -α3.7-Hb G-Philadelphia
Comments: The missense mutation Hb G-Philadelphia [IthaID: 596] was found on a chromosome that carries -α3.7 (type I) [IthaID: 300], in a homozygous case for the -α3.7 deletion. Reported as both an AAC>AAA or AAG change [Asn>Lys].
We follow the HGVS sequence variant nomenclature and IUPAC standards.
External Links
No available links
Phenotype
Hemoglobinopathy Group: | Thalassaemia and Structural Haemoglobinopathy |
---|---|
Hemoglobinopathy Subgroup: | α-thalassaemia, α-chain variant |
Allele Phenotype: | α⁺ |
Stability: | N/A |
Oxygen Affinity: | N/A |
Associated Phenotypes: | N/A |
Location
Chromosome: | 16 |
---|---|
Locus: | NG_000006.1 |
Locus Location: | 34099 or 34247 |
Size: | 1 bp or 3.804 kb |
Located at: | α2, α3.7 hybrid |
Other details
Type of Mutation: | Combination |
---|---|
Ethnic Origin: | N/A |
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
- Molchanova TP, Pobedimskaya DD, Ye Z, Huisman TH, Two different mutations in codon 68 are observed in Hb G-Philadelphia heterozygotes., Am. J. Hematol. , 45(4), 345-6, 1994 PubMed
Microattributions
A/A | Contributor(s) | Date | Comments |
---|---|---|---|
1 | Papasavva, Thessalia | 2022-09-23 | First report. AAC>AAA change |
Created on 2022-09-23 12:01:53,
Last reviewed on 2024-03-08 10:59:25 (Show full history)
A/A | Date | Curator(s) | Comments |
---|---|---|---|
1 | 2022-09-23 12:01:53 | The IthaGenes Curation Team | Created |
2 | 2022-09-26 15:03:22 | The IthaGenes Curation Team | Reviewed. Synonym added. |
3 | 2022-09-28 11:40:18 | The IthaGenes Curation Team | Reviewed. Allele phenotype added. |
4 | 2024-03-06 09:33:54 | The IthaGenes Curation Team | Reviewed. HGVS name corrected |
5 | 2024-03-06 10:33:17 | The IthaGenes Curation Team | Reviewed. Reference added |
6 | 2024-03-06 10:58:28 | The IthaGenes Curation Team | Reviewed. |
7 | 2024-03-06 14:19:21 | The IthaGenes Curation Team | Reviewed. |
8 | 2024-03-06 14:20:50 | The IthaGenes Curation Team | Reviewed. Location |
9 | 2024-03-06 14:21:26 | The IthaGenes Curation Team | Reviewed. |
10 | 2024-03-06 15:01:40 | The IthaGenes Curation Team | Reviewed. |
11 | 2024-03-06 15:02:57 | The IthaGenes Curation Team | Reviewed. |
12 | 2024-03-08 10:59:25 | The IthaGenes Curation Team | Reviewed. Comment added |
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IthaGenes was last updated on 2024-11-20 13:24:07