IthaID: 180


Names and Sequences

Functionality: Globin gene causative mutation Pathogenicity: Pathogenic / Likely Pathogenic
Common Name: CD 76 GCT>--T (-GC) HGVS Name: HBB:c.229_230delGC
Hb Name: N/A Protein Info: β 76 (-GC); modified C-terminal sequence

Context nucleotide sequence:
GCTCGGTGCCTTTAGTGATGGCCTG [-/GC] TCACCTGGACAACCTCAAGGGCACC (Strand: -)

Also known as:

We follow the HGVS sequence variant nomenclature and IUPAC standards.

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: 70953
Size: 2 bp
Located at: β
Specific Location: Exon 2

Other details

Type of Mutation: Point-Mutation(Deletion)
Effect on Gene/Protein Function: Frameshift (Translation)
Ethnic Origin: North African
Molecular mechanism: N/A
Inheritance: Recessive
DNA Sequence Determined: No

In silico pathogenicity prediction

Publications / Origin

  1. Foulon K, Rochette J, Cadet E, A novel beta-Thalassemic allele due to a two nucleotide deletion: beta76 (-GC)., Hemoglobin, 31(1), 31-7, 2007
Created on 2010-06-16 16:13:15, Last reviewed on 2014-04-08 12:59:04 (Show full history)

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