Variant position: 142 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 355 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 RSNDGNSYRLQSWLYSSRLL QYSDALEHLLTTGQGVVLERS
Gorilla RSNDGNSYRLQSWLYSSRLL QYSDALEHLLTTGQGVVLERS
Chimpanzee RSNDGNSYRLQSWLYSSRLL QYSDALEHLLTTGQGVVLERS
Mouse KSNDGNSYRLQSWLYASRLL QYADALEHLLSTGQGVVLERS
Rat KSNDGNSYRLQSWLYASRLL QYSDALEHLLSTGQGVVLERS
Bovine KSNDGNSYRLQAWLYASRLL QYADALEHLLSTGQGVVLERS
Drosophila SHDLAAQFQIR--MYMLRYS QYIDALQHVLSTGQGVVLERS
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
36 – 355 NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 10, mitochondrial
NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease.
Hoefs S.J.; van Spronsen F.J.; Lenssen E.W.; Nijtmans L.G.; Rodenburg R.J.; Smeitink J.A.; van den Heuvel L.P.;
Eur. J. Hum. Genet. 19:270-274(2011)
Cited for: INVOLVEMENT IN MC1DN22; VARIANT MC1DN22 ARG-142;
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.