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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q93009: Variant p.Ile766Thr

Ubiquitin carboxyl-terminal hydrolase 7
Gene: USP7
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Variant information Variant position: help 766 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance
Residue change: help From Isoleucine (I) to Threonine (T) at position 766 (I766T, p.Ile766Thr). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from medium size and hydrophobic (I) to medium size and polar (T) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -1 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page
Variant description: help In HAFOUS. Any additional useful information about the variant.


Sequence information Variant position: help 766 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1102 The length of the canonical sequence.
Location on the sequence: help IQDYDVSLDKALDELMDGDI I VFQKDDPENDNSELPTAKEY 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         IQDYDVSLDKAL---DELMDGDIIVFQKDDPENDNSEL-PTAKEY

Mouse                         IQDYDVSLDKAL---DELMDGDIIVFQKDDPENDNSEL-PT

Rat                           IQDYDVSLDKAL---DELMDGDIIVFQKDDPENDNSEL-PT

Chicken                       IQDYDVSLDKAL---DELMDGDIIVFQKDDPENDSSEL-PT

Caenorhabditis elegans        VDLTQNYSIGRL---VEEQDGGILVVEKVETSTSTQNAKQK

Drosophila                    LVNLNEPIESALFIPQDHLQGHILIFERENVDAKL-DL-PT

Baker's yeast                 QHVANDYPNLLLYNADALKVSNNEYKHWFDKNVIGNGISPI

Fission yeast                 TDQAPTTNSSSL--NENLLGGHASENDKSLKQSPFQKLTRR
Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 1 – 1102 Ubiquitin carboxyl-terminal hydrolase 7
Region 622 – 801 Interaction with ICP0/VMW110
Beta strand 764 – 770



Literature citations
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.
Fountain M.D.; Oleson D.S.; Rech M.E.; Segebrecht L.; Hunter J.V.; McCarthy J.M.; Lupo P.J.; Holtgrewe M.; Moran R.; Rosenfeld J.A.; Isidor B.; Le Caignec C.; Saenz M.S.; Pedersen R.C.; Morgan T.M.; Pfotenhauer J.P.; Xia F.; Bi W.; Kang S.L.; Patel A.; Krantz I.D.; Raible S.E.; Smith W.; Cristian I.; Torti E.; Juusola J.; Millan F.; Wentzensen I.M.; Person R.E.; Kuery S.; Bezieau S.; Uguen K.; Ferec C.; Munnich A.; van Haelst M.; Lichtenbelt K.D.; van Gassen K.; Hagelstrom T.; Chawla A.; Perry D.L.; Taft R.J.; Jones M.; Masser-Frye D.; Dyment D.; Venkateswaran S.; Li C.; Escobar L.F.; Horn D.; Spillmann R.C.; Pena L.; Wierzba J.; Strom T.M.; Parenti I.; Kaiser F.J.; Ehmke N.; Schaaf C.P.;
Genet. Med. 21:1797-1807(2019)
Cited for: VARIANTS HAFOUS ILE-225; LYS-345; PHE-373; ASP-392; GLY-485; 576-CYS--ASN-1102 DEL; PRO-757; THR-766 AND ASN-1080; INVOLVEMENT IN HAFOUS;
Disclaimer: 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.