IthaID: 151


Names and Sequences

Functionality: Globin gene causative mutation Pathogenicity: Pathogenic / Likely Pathogenic
Common Name: CD 44 -C HGVS Name: HBB:c.135delC
Hb Name: N/A Protein Info: β 44 (-C); modified C-terminal sequence: (44)Ser-Leu-Gly-Ile-Cys-Pro-Leu-Leu-Met-Leu- Leu-Trp-Ala-Thr-Leu-(59)Arg-COOH

Context nucleotide sequence:
CTTGGACCCAGAGGTTCTTTGAGTC [-/C] TTTGGGGATCTGTCCACTCCTGATG (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: 70859
Size: 1 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: Kurdish
Molecular mechanism: N/A
Inheritance: Recessive
DNA Sequence Determined: No

In silico pathogenicity prediction

Frequencies

Publications / Origin

  1. Kinniburgh AJ, Maquat LE, Schedl T, Rachmilewitz E, Ross J, mRNA-deficient beta o-thalassemia results from a single nucleotide deletion., Nucleic acids research, 10(18), 5421-7, 1982
  2. Rund D, Cohen T, Filon D, Dowling CE, Warren TC, Barak I, Rachmilewitz E, Kazazian HH, Oppenheim A, Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan., Proceedings of the National Academy of Sciences of the United States of America, 88(1), 310-4, 1991
Created on 2010-06-16 16:13:15, Last reviewed on 2014-05-12 09:26:13 (Show full history)

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