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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot O75419: Variant p.Glu155Gly

Cell division control protein 45 homolog
Gene: CDC45
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Variant information Variant position: help 155 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help US 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 Glutamate (E) to Glycine (G) at position 155 (E155G, p.Glu155Gly). 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 acidic (E) to glycine (G) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -2 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 MGORS7; uncertain significance; associated in cis with T-321. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 155 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 566 The length of the canonical sequence.
Location on the sequence: help RDEEEDEEHSGNDSDGSEPS E KRTRLEEEIVEQTMRRRQRR 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                         RDEEEDEEHSGNDSDGSEPSEKRTRLEEEIVEQTM-RRRQRR

Mouse                         RDEAEDEDLSDSDGDGSEPSEKRTRLEEEIVERNR-KRRQR

Xenopus laevis                NDDEEDGEDSGNESDGAEPSGKRRRFDEAAVERRIERRRQR

Slime mold                    DPENEDNPENDEDDGGSENIDENERKSKKKNKKDKKSKRKH

Baker's yeast                 DEATDADEVTDEDEEDEDETISNKRGNSSIGPNDLSKRKQR

Fission yeast                 EEEVEDDNRSVESYSSSDYQARSRRRFSEETTQRRAEIKEK

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 – 566 Cell division control protein 45 homolog
Region 136 – 163 Disordered
Compositional bias 147 – 163 Basic and acidic residues
Modified residue 144 – 144 Phosphoserine
Modified residue 148 – 148 Phosphoserine



Literature citations
Mutations in CDC45, encoding an essential component of the pre-initiation complex, cause Meier-Gorlin syndrome and craniosynostosis.
Fenwick A.L.; Kliszczak M.; Cooper F.; Murray J.; Sanchez-Pulido L.; Twigg S.R.; Goriely A.; McGowan S.J.; Miller K.A.; Taylor I.B.; Logan C.; Bozdogan S.; Danda S.; Dixon J.; Elsayed S.M.; Elsobky E.; Gardham A.; Hoffer M.J.; Koopmans M.; McDonald-McGinn D.M.; Santen G.W.; Savarirayan R.; de Silva D.; Vanakker O.; Wall S.A.; Wilson L.C.; Yuregir O.O.; Zackai E.H.; Ponting C.P.; Jackson A.P.; Wilkie A.O.; Niedzwiedz W.; Bicknell L.S.;
Am. J. Hum. Genet. 99:125-138(2016)
Cited for: INVOLVEMENT IN MGORS7; VARIANTS MGORS7 ARG-68; HIS-76; GLY-155; CYS-157; GLY-226; TYR-264; VAL-298; THR-321; 424-ARG--SER-566 DEL; LEU-463; LEU-496 AND TRP-554; CHARACTERIZATION OF VARIANTS MGORS7 ARG-68; HIS-76; CYS-157; GLY-226 AND VAL-298;
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.