IthaID: 1327


Names and Sequences

Functionality: Globin gene causative mutation Pathogenicity: N/A
Common Name: -36 (C>A) HGVS Name: HBD:c.-86C>A
Hb Name: N/A Protein Info: N/A

Context nucleotide sequence:
GCTCACTGGAGCAGGGAGGACAGGA [A/C] CAGCATAAAAGGCAGGGCAGAGTCG (Strand: -)

Also known as:

We follow the HGVS sequence variant nomenclature and IUPAC standards.

External Links

Phenotype

Hemoglobinopathy Group: Thalassaemia
Hemoglobinopathy Subgroup: δ-thalassaemia
Allele Phenotype:δ+
Associated Phenotypes: N/A

Location

Chromosome: 11
Locus: NG_000007.3
Locus Location: 63097
Size: 1 bp
Located at: δ
Specific Location: Promoter

Other details

Type of Mutation: Point-Mutation(Substitution)
Effect on Gene/Protein Function: N/A
Ethnic Origin: Greek
Molecular mechanism: N/A
Inheritance: Recessive
DNA Sequence Determined: Yes

In silico pathogenicity prediction

Publications / Origin

  1. Papadakis M, Papapanagiotou E, Loutradi-Anagnostou A, Scanning method to identify the molecular heterogeneity of delta-globin gene especially in delta-thalassemias: detection of three novel substitutions in the promoter region of the gene., Human mutation, 9(5), 465-72, 1997
Created on 2010-06-16 16:13:17, Last reviewed on 2013-10-15 17:28:32 (Show full history)

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