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UniProtKB/Swiss-Prot Q03431: Variant p.Arg150Cys

Parathyroid hormone/parathyroid hormone-related peptide receptor
Gene: PTH1R
Variant information

Variant position:  150
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  LB/B
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:  From Arginine (R) to Cysteine (C) at position 150 (R150C, p.Arg150Cys).
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:  Change from large size and basic (R) to medium size and polar (C)
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  -3
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

Other resources:  
Links to websites of interest for the variant.



Sequence information

Variant position:  150
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  593
The length of the canonical sequence.

Location on the sequence:   PCPDYIYDFNHKGHAYRRCD  R NGSWELVPGHNRTWANYSEC
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                         PCPDYIYDFNHKGHAYRRCDRNGSWELVPGHNRTWANYSEC

                              PCPDYIYDFNHKGHAYRRCDRNGSWELVPGHNRTWANYSEC

Mouse                         PCPDYIYDFNHKGHAYRRCDRNGSWEVVPGHNRTWANYSEC

Rat                           PCPDYIYDFNHKGHAYRRCDRNGSWEVVPGHNRTWANYSEC

Pig                           PCPDYIYDFNHKGHAYRRCDRNGSWELVPGHNRTWANYSEC

Bovine                        PCPDYIYDFNHKGHAYRRCDRNGSWELVPGHNRTWANYSEC

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.

TypePositionsDescription
Chain 27 – 593 Parathyroid hormone/parathyroid hormone-related peptide receptor
Topological domain 27 – 188 Extracellular
Glycosylation 151 – 151 N-linked (GlcNAc...) asparagine
Glycosylation 161 – 161 N-linked (GlcNAc...) asparagine
Glycosylation 166 – 166 N-linked (GlcNAc...) asparagine
Disulfide bond 131 – 170
Mutagenesis 135 – 135 I -> K. Abolishes hormone binding and homodimerization.
Mutagenesis 137 – 137 D -> A. Abolishes hormone binding. No effect on homodimerization.


Literature citations

A mutant PTH/PTHrP type I receptor in enchondromatosis.
Hopyan S.; Gokgoz N.; Poon R.; Gensure R.C.; Yu C.; Cole W.G.; Bell R.S.; Jueppner H.; Andrulis I.L.; Wunder J.S.; Alman B.A.;
Nat. Genet. 30:306-310(2002)
Cited for: VARIANT CYS-150;

Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C.
Rozeman L.B.; Sangiorgi L.; Briaire-de Bruijn I.H.; Mainil-Varlet P.; Bertoni F.; Cleton-Jansen A.-M.; Hogendoorn P.C.W.; Bovee J.V.M.G.;
Hum. Mutat. 24:466-473(2004)
Cited for: DISCUSSION OF THE ASSOCIATION OF CYS-150 WITH ENCHONDROMATOSIS;

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.