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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q96AG3: Variant p.Pro333Leu

Mitochondrial outer membrane protein SLC25A46
Gene: SLC25A46
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Variant information Variant position: help 333 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance
Residue change: help From Proline (P) to Leucine (L) at position 333 (P333L, p.Pro333Leu). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Similar physico-chemical property. Both residues are medium size and hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -3 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page
Variant description: help In HMSN6B; decreased protein abundance. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 333 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 418 The length of the canonical sequence.
Location on the sequence: help YFPELIANFAASLCSDVILY P LETVLHRLHIQGTRTIIDNT 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         YFPELIANFAASLCSDVILYPLETVLHRLHIQGTRTIIDNT

Mouse                         YFPELIANFAASLCSDVILYPLETVLHRLHIQGTRTIIDNT

Rat                           YFPELIANFAASLCSDVILYPLETVLHRLHIQGTRTIIDNT

Chicken                       YFPELIASFAASLCADVMLYPLETVLHRLHIQGTRTIIDNT

Xenopus tropicalis            YFPELIANFAASLCADVLLYPLETVLHRLHIQGTRTIIDNT

Zebrafish                     YFPELMASFAASLCADVLLFPLETVLHRLHIQGTRTIIDNT
Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 1 – 418 Mitochondrial outer membrane protein SLC25A46
Transmembrane 314 – 334 Helical; Name=5
Repeat 311 – 413 Solcar 2



Literature citations
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
Abrams A.J.; Hufnagel R.B.; Rebelo A.; Zanna C.; Patel N.; Gonzalez M.A.; Campeanu I.J.; Griffin L.B.; Groenewald S.; Strickland A.V.; Tao F.; Speziani F.; Abreu L.; Schuele R.; Caporali L.; La Morgia C.; Maresca A.; Liguori R.; Lodi R.; Ahmed Z.M.; Sund K.L.; Wang X.; Krueger L.A.; Peng Y.; Prada C.E.; Prows C.A.; Schorry E.K.; Antonellis A.; Zimmerman H.H.; Abdul-Rahman O.A.; Yang Y.; Downes S.M.; Prince J.; Fontanesi F.; Barrientos A.; Nemeth A.H.; Carelli V.; Huang T.; Zuchner S.; Dallman J.E.;
Nat. Genet. 47:926-932(2015)
Cited for: FUNCTION; SUBCELLULAR LOCATION; INTERACTION WITH IMMT; INVOLVEMENT IN HMSN6B; VARIANTS HMSN6B ASP-249; LEU-333; ASP-335 AND CYS-340; Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia.
Wan J.; Steffen J.; Yourshaw M.; Mamsa H.; Andersen E.; Rudnik-Schoeneborn S.; Pope K.; Howell K.B.; McLean C.A.; Kornberg A.J.; Joseph J.; Lockhart P.J.; Zerres K.; Ryan M.M.; Nelson S.F.; Koehler C.M.; Jen J.C.;
Brain 139:2877-2890(2016)
Cited for: INVOLVEMENT IN PCH1E; VARIANT PCH1E PRO-341; CHARACTERIZATION OF VARIANT PCH1E PRO-341; CHARACTERIZATION OF VARIANTS HMSN6B ASP-249; LEU-333; ASP-335; CYS-340; FUNCTION; SUBCELLULAR LOCATION;
Disclaimer: 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.