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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9BZH6: Variant p.Phe1150Leu

WD repeat-containing protein 11
Gene: WDR11
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Variant information Variant position: help 1150 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 Phenylalanine (F) to Leucine (L) at position 1150 (F1150L, p.Phe1150Leu). 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 medium size and hydrophobic (L) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 0 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 HH14; does not affect the subcellular location of the protein; decreases capacity to shuttle from cilium to nucleus; decreases GLI3 protein levels. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 1150 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1224 The length of the canonical sequence.
Location on the sequence: help VLLSLGCFFSVAETLHSMRY F DRAALFVEACLKYGAFEVTE 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                         VLLSLGCFFSVAETLHSMRYFDRAALFVEACLKYGAFEVTE

Mouse                         VLLSLGCFVSVAETLHSMRYFDRAALFVEACLKYGAFEVSE

Zebrafish                     VLLSLGCFQKVGEMLHSMRYFDRAALFIEACLKYGVMETND
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 – 1224 WD repeat-containing protein 11



Literature citations
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
Kim H.G.; Ahn J.W.; Kurth I.; Ullmann R.; Kim H.T.; Kulharya A.; Ha K.S.; Itokawa Y.; Meliciani I.; Wenzel W.; Lee D.; Rosenberger G.; Ozata M.; Bick D.P.; Sherins R.J.; Nagase T.; Tekin M.; Kim S.H.; Kim C.H.; Ropers H.H.; Gusella J.F.; Kalscheuer V.; Choi C.Y.; Layman L.C.;
Am. J. Hum. Genet. 87:465-479(2010)
Cited for: SUBCELLULAR LOCATION; CHROMOSOMAL TRANSLOCATION; INTERACTION WITH EMX1; VARIANTS HH14 TRP-395; THR-435; GLN-448; GLN-690 AND LEU-1150; VARIANT GLN-978; CHARACTERIZATION OF VARIANTS HH14 TRP-395; THR-435; GLN-448; GLN-690 AND LEU-1150; WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome.
Kim Y.J.; Osborn D.P.; Lee J.Y.; Araki M.; Araki K.; Mohun T.; Kaensaekoski J.; Brandstack N.; Kim H.T.; Miralles F.; Kim C.H.; Brown N.A.; Kim H.G.; Martinez-Barbera J.P.; Ataliotis P.; Raivio T.; Layman L.C.; Kim S.H.;
EMBO Rep. 19:269-289(2018)
Cited for: FUNCTION; SUBCELLULAR LOCATION; INTERACTION WITH EMX1 AND GLI3; VARIANT HH14 LEU-537; CHARACTERIZATION OF VARIANTS HH14 TRP-395; THR-435; GLN-448; LEU-537; GLN-690 AND LEU-1150;
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.