Variant position: 590 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 960 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 TRFNLETEWKNNYPRLRELD RNELFEKAKNEILDEVISLSQ
Mouse TRFNLETEWKNNYPRLRELD RNELFEKAKNEILDEVISLSQ
Rat TRFNLETEWKNNYPRLRELD RNELFEKAKNEILDEVISLSQ
Chicken TRFNLETEWKNNYPRLRELD RNELFEKAKNEILDEVISLTQ
Zebrafish SRFNLETEWKNNYPRLRELD RNELYEKAKNEILDEVISLSQ
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
88 – 960 Dynamin-like 120 kDa protein, mitochondrial
195 – 960 Dynamin-like 120 kDa protein, form S1
114 – 960 Mitochondrial intermembrane
Dominant optic atrophy: correlation between clinical and molecular genetic studies.
Puomila A.; Huoponen K.; Maentyjaervi M.; Haemaelaeinen P.; Paananen R.; Sankila E.-M.; Savontaus M.-L.; Somer M.; Nikoskelainen E.;
Acta Ophthalmol. Scand. 83:337-346(2005)
Cited for: VARIANTS OPA1 324-ARG--PRO-326 DEL; TRP-590 AND LYS-728; VARIANT ASN-158;
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.