Variant position: 105 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 320 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 HKVPQFHGKWPFSRFLFFQE PASAVASFLNGLASLVMLCRY
Mouse HRVPQFHGKWPFSRFLFIQE PASAVASLLNGLASLVMLCRY
Bovine QKVPQFHGKWPFSRFLCFQE PASAVASFLNGLASLVMLCRY
Xenopus laevis HEVPQFHGKWPFSRFLFFQE PASALASFLNGVASLLMLFRY
Xenopus tropicalis HEVPQFHGKWPFSRFLFFQE PASALASFLNGVASLLMLLRY
Zebrafish YSIPQFHGKWPFARFLCFEE PASALASLLNGLACLLMLLRY
Drosophila WPIPQFYGKWPFLRLLGMQE PASVIFSCLNFVVHLRLLRKF
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
21 – 320 Post-GPI attachment to proteins factor 3
99 – 119 Helical
94 – 144 Missing. In isoform 2.
Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation.
Howard M.F.; Murakami Y.; Pagnamenta A.T.; Daumer-Haas C.; Fischer B.; Hecht J.; Keays D.A.; Knight S.J.; Kolsch U.; Kruger U.; Leiz S.; Maeda Y.; Mitchell D.; Mundlos S.; Phillips J.A.; Robinson P.N.; Kini U.; Taylor J.C.; Horn D.; Kinoshita T.; Krawitz P.M.;
Am. J. Hum. Genet. 94:278-287(2014)
Cited for: VARIANTS HPMRS4 ASP-92; ARG-105 AND GLY-305; CHARACTERIZATION OF VARIANTS HPMRS4 ASP-92; ARG-105 AND GLY-305;
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.