
IthaID: 718
Names and Sequences
| Functionality: | Globin gene causative mutation | Pathogenicity: | N/A | 
|---|---|---|---|
| Common Name: | CD 116 GAG>CAG [Glu>Gln] | HGVS Name: | HBA1:c.349G>C | HBA2:c.349G>C | 
| Hb Name: | Hb Oleander | Protein Info: | α2 or α1 116(GH4) Glu>Gln | 
| Also known as: | 
We follow the 
						 
							HGVS sequence variant nomenclature
						
						and
						 
							 IUPAC standards.
						
					
					
					
Context nucleotide sequence:
GACCCTGGCCGCCCACCTCCCCGCC [A/C/G] AGTTCACCCCTGCGGTGCACGCCTC  (Strand: +)
Protein sequence:
MVLSPADKTNVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHGKKVADALTNAVAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAQFTPAVHASLDKFLASVSTVLTSKYR
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: | 34383 or 38194 | 
| Size: | 1 bp or 1 bp | 
| Located at: | α1 or α2 | 
| Specific Location: | Exon 3 | 
Other details
| Type of Mutation: | Point-Mutation(Substitution) | 
|---|---|
| Effect on Gene/Protein Function: | Missense codons (Protein Structure) | 
| Ethnic Origin: | African | 
| Molecular mechanism: | N/A | 
| Inheritance: | Recessive | 
| DNA Sequence Determined: | No | 
In silico pathogenicity prediction
Publications / Origin
- Schneider RG, Hightower B, Carpentieri U, Duerst ML, Shih T, Jones RT, Hemoglobin Oleander [alpha 116(GH4)Glu replaced by Gln beta 2]: structural and functional characterization., Hemoglobin , 6(5), 465-80, 1982
					Created on 2010-06-16 16:13:16,
					Last reviewed on 2014-04-14 17:30:02					(Show full history)
				
				
			
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