Variant position: 142 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 451 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 TWQNFDSLLIPADHPSRKKG DNYYLNRTHMLRAHTSAHQ----WD
Mouse TWQNFDSLLIPADHPSRKKG DNYYLNRAHMLRAHTSAHQ--
Rat TWQNFDSLLIPADHPSRKKG DNYYLNRGHMLRAHTSAHQ--
Drosophila VQQNFDNLLIPADHVSRQKS DCYYINQQHLLRAHTTAHQ--
Slime mold VKENFDELLFPVDHVGRSPN DTYYFSKDQLLRTHTSAHQ--
Baker's yeast TMENFDSLGFPKDHPGRSKS DTYYINETHLLRTHTSAHELE
Fission yeast VETNFDSLGFPKTHVSRSKS DTYYMNNKTCLRTHTSAHQPE
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.
A newly identified missense mutation in FARS2 causes autosomal-recessive spastic paraplegia.
Yang Y.; Liu W.; Fang Z.; Shi J.; Che F.; He C.; Yao L.; Wang E.; Wu Y.;
Hum. Mutat. 37:165-169(2016)
Cited for: VARIANT SPG77 TYR-142; CHARACTERIZATION OF VARIANT SPG77 TYR-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.