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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot O00358: Variant p.Phe137Ser

Forkhead box protein E1
Gene: FOXE1
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Variant information Variant position: help 137 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 Phenylalanine (F) to Serine (S) at position 137 (F137S, p.Phe137Ser). 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 large size and aromatic (F) to small size and polar (S) 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 congenital hypothyroidism; loss of sequence-specific DNA binding; loss of transcriptional activity. Any additional useful information about the variant.


Sequence information Variant position: help 137 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 373 The length of the canonical sequence.
Location on the sequence: help EAGRPGKGNYWALDPNAEDM F ESGSFLRRRKRFKRSDLSTY 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                         EAGRPGKGNYWALDPNAEDMFESGSFLRRRKRFKRSDLSTY

Mouse                         EAGRPGKGNYWALDPNAEDMFESGSFLRRRKRFKRSDLSTY

Xenopus laevis                EPGRPGKGNYWALDPNAEDMFDSGSFLRRRKRFKRTDLTTY

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 – 373 Forkhead box protein E1
DNA binding 53 – 147 Fork-head



Literature citations
MSX1 and TGF-beta3 are novel target genes functionally regulated by FOXE1.
Venza I.; Visalli M.; Parrillo L.; De Felice M.; Teti D.; Venza M.;
Hum. Mol. Genet. 20:1016-1025(2011)
Cited for: FUNCTION; SUBCELLULAR LOCATION; CHARACTERIZATION OF VARIANTS BAMLAZ ASN-57 AND VAL-65; CHARACTERIZATION OF VARIANTS CONGENITAL HYPOTHYROIDISM CYS-102 AND SER-137; Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism.
Castanet M.; Mallya U.; Agostini M.; Schoenmakers E.; Mitchell C.; Demuth S.; Raymond F.L.; Schwabe J.; Gurnell M.; Chatterjee V.K.;
J. Clin. Endocrinol. Metab. 95:4031-4036(2010)
Cited for: VARIANT CONGENITAL HYPOTHYROIDISM SER-137; CHARACTERIZATION OF VARIANT CONGENITAL HYPOTHYROIDISM SER-137; FUNCTION;
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.