Variant position: 71 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 622 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 RGLLHSLQGLPAAVPVLPLE LTVTCNFIILRASLAQGFTED
Mouse RELLLTLQGLPAAVPALPLE LTVLCNCIILRASLVQAFTED
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 – 622 Fanconi anemia group G protein
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
Demuth I.; Wlodarski M.; Tipping A.J.; Morgan N.V.; de Winter J.P.; Thiel M.; Grasl S.; Schindler D.; D'Andrea A.D.; Altay C.; Kayserili H.; Zatterale A.; Kunze J.; Ebell W.; Mathew C.G.; Joenje H.; Sperling K.; Digweed M.;
Eur. J. Hum. Genet. 8:861-868(2000)
Cited for: VARIANT FANCG PRO-71;
HES1 is a novel interactor of the Fanconi anemia core complex.
Tremblay C.S.; Huang F.F.; Habi O.; Huard C.C.; Godin C.; Levesque G.; Carreau M.;
Cited for: VARIANT FANCG PRO-71; INTERACTION WITH HES1; SUBCELLULAR LOCATION; MUTAGENESIS OF GLY-546;
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