Variant position: 382 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 701 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human PGPDCPIFLPSDSEWDWLLA KTWVRYAEFYSHEAIAHLLET
Mouse PGPDCPIFLPNDSEWDWLLA KTWVRYAEFYSHEAVAHLLES
Rat PGPDCPIFLPNDSEWDWLLA KTWVRYAEFYSHEAVAHLLES
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
1 – 701 Arachidonate 12-lipoxygenase, 12R-type
120 – 701 Lipoxygenase
398 – 398 Iron; catalytic
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.
Eckl K.M.; de Juanes S.; Kurtenbach J.; Naetebus M.; Lugassy J.; Oji V.; Traupe H.; Preil M.L.; Martinez F.; Smolle J.; Harel A.; Krieg P.; Sprecher E.; Hennies H.C.;
J. Invest. Dermatol. 129:1421-1428(2009)
Cited for: VARIANTS ARCI2 LEU-195 AND GLU-382; CHARACTERIZATION OF VARIANTS ARCI2 LEU-195 AND GLU-382;
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.