IthaID: 819

Names and Sequences

Functionality: Globin gene causative mutation
Common Name: CD 6 GAG>GTG; CD 142 GCC>GTC HGVS Name: HBB:c.[20A>T;428C>T]
Hb Name: Hb S-Travis Protein Info: β 6(A3) Glu>Val AND β 142(H20) Ala>Val

Context nucleotide sequence:

Protein sequence:

Also known as:

External Links


Chromosome: 11
Locus: NG_000007.3
Locus Location: 70614
Size: 1 bp
Located at: β
Specific Location: Exon 1


Hemoglobinopathy Group: Structural Haemoglobinopathy
Hemoglobinopathy Subgroup: β-chain variant
Allele Phenotype:Sickling
Stability: Unstable
Oxygen Affinity: Increased Oxygen Affinity
Associated Phenotypes: N/A

Other details

Type of Mutation: Point-Mutation(Substitution)
Effect on Gene/Protein Function: N/A
Ethnic Origin: African
Inheritance: Recessive
DNA Sequence Determined: No

Sequence Viewer

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Publications / Origin

  1. Moo-Penn WF, Schmidt RM, Jue DL, Bechtel KC, Wright JM, Horne MK, Haycraft GL, Roth EF, Nagel RL, Hemoglobin S Travis: a sickling hemoglobin with two amino acid substitutions [beta6(A3)glutamic acid leads to valine and beta142 (h20) alanine leads to valine)., European journal of biochemistry / FEBS, 77(3), 561-6, 1977 PubMed
Created on 2010-06-16 16:13:16, Last reviewed on 2013-10-15 17:00:14 (Show full history)

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