Variant position: 418 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 561 The length of the canonical sequence.
Location on the sequence:
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 RPAVLPRPEKPQLPHLQRSP PDGQSFRSFSFEKPRQPSQAD
Mouse RPAVLPRPENTPLPHLQRSP PDGQSFRGFSFEKARQPSQAD
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.
Type Positions Description
1 – 561 SH3 domain-binding protein 2
333 – 451 Disordered
415 – 438 Polar residues
416 – 416 Phosphoserine
427 – 427 Phosphoserine
98 – 561 Missing. In isoform 2.
Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism.
Ueki Y.; Tiziani V.; Santanna C.; Fukai N.; Maulik C.; Garfinkle J.; Ninomiya C.; doAmaral C.; Peters H.; Habal M.; Rhee-Morris L.; Doss J.B.; Kreiborg S.; Olsen B.R.; Reichenberger E.;
Nat. Genet. 28:125-126(2001)
Cited for: VARIANTS CRBM GLN-415; PRO-415; ARG-418; HIS-418; LEU-418; ARG-420 AND GLU-420;
A missense mutation in the SH3BP2 gene on chromosome 4p16.3 found in a case of nonfamilial cherubism.
Imai Y.; Kanno K.; Moriya T.; Kayano S.; Seino H.; Matsubara Y.; Yamada A.;
Cleft Palate Craniofac. J. 40:632-638(2003)
Cited for: VARIANT CRBM ARG-418;
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