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Blood, Vol. 101, Issue 6, 2081-2087, March 15, 2003
The molecular genetics of the human I locus and molecular background explain the partial association of the adult i phenotype with congenital cataracts
Blood Yu et al.
101: 2081
Supplemental materials for: Yu et al, Vol 101, Issue 6, 2081-2088
Figure S1. Nucleotide sequences for IGnTA, IGnTB, and IGnTC cDNA (PDF, 25KB). The translation start and stop codons are boxed. The translation start codons are numbered 1-3. The exon 1–exon 2 and exon 2–exon 3 junctions are indicated by arrows. It was demonstrated that the IGnTA and IGnTB transcripts had the same 3'-untranslated region (longest); however, the 3'-untranslated region of the IGnTC transcript was shorter. The sequences for IGnTA, IGnTB, and IGnTC cDNA have been submitted to the GenBank/EBI Data Bank with accession numbers AF458024, AF458025, and AF458026, respectively.
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