Variant position: 586 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 769 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 PGFEGSACQCERTTEGCLNP RRVECSGRGRCRCNVCECHSG
Mouse PGYEGSACQCQRSTTGCLNA RLVECSGRGHCQCNRCICDEG
Pig EGFEGSACQCLKSTQGCLNL QGVECSGRGRCRCNVCQCDFG
Bovine EQYEGSACQCLKSTQGCLNL DGVECSGRGRCRCNVCQCDPG
Goat EQHEGSACQCLKSTQGCLNL DGVECSGRGRCRCNVCQCDPG
Sheep DQHEGSACQCLKSTQGCLNL DGVECSGRGRCRCNVCQCDPG
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.
Genetic cause of leukocyte adhesion molecule deficiency. Abnormal splicing and a missense mutation in a conserved region of CD18 impair cell surface expression of beta 2 integrins.
Nelson C.; Rabb H.; Arnaout M.A.;
J. Biol. Chem. 267:3351-3357(1992)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 347-355; VARIANTS LAD1 SER-351 AND TRP-586; VARIANT HIS-354;
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.