Variant position: 43 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 348 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 RLLRSHSLHYLFMGASEQDL GLSLFEALGYVDDQLFVFYDH
Chimpanzee RLLRSHSLHYLFMGASEQDL GLSLFEALGYVDDQLFVFYDH
Mouse LPPRSHSLRYLFMGASEPDL GLPLFEARGYVDDQLFVSYNH
Rat LRPGSHSLRYLFMGASKPDL GLPFFEALGYVDDQLFVSYNH
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
23 – 348 Hereditary hemochromatosis protein
23 – 306 Extracellular
23 – 114 Alpha-1
26 – 114 RSHSLHYLFMGASEQDLGLSLFEALGYVDDQLFVFYDHESRRVEPRTPWVSSRISSQMWLQLSQSLKGWDHMFTVDFWTIMENHNHSKE -> Q. In isoform 2 and isoform 4.
26 – 49 RSHSLHYLFMGASEQDLGLSLFEA -> P. In isoform 5.
26 – 26 R -> Q. In isoform 11.
26 – 26 R -> L. In isoform 6.
27 – 298 Missing. In isoform 11.
27 – 206 Missing. In isoform 6.
43 – 45
An unusual case of hemochromatosis due to a new compound heterozygosity in HFE (p.[Gly43Asp;His63Asp]+[Cys282Tyr]): structural implications with respect to binding with transferrin receptor 1.
Dupradeau F.-Y.; Pissard S.; Coulhon M.-P.; Cadet E.; Foulon K.; Fourcade C.; Goossens M.; Case D.A.; Rochette J.;
Hum. Mutat. 29:206-206(2008)
Cited for: VARIANTS HFE1 ASP-43 AND TYR-282; VARIANT ASP-63;
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.