Sequence information
Variant position: 294 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 305 The length of the canonical sequence.
Location on the sequence:
KDIDLASQPVYCNLQSLGQA
P MDEEEYVIPGH
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 KDIDLASQPVYCNLQSLGQAP MDEEEYVIPGH
Mouse RSVDQDSQPVYCNLESLGR-- -----------
Bovine DSLQHESQPVYCNLQSLSQVP LDDEEYVVPGR
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
Chain
21 – 305
Leucine-rich repeat-containing protein 25
Topological domain
187 – 305
Cytoplasmic
Modified residue
284 – 284
Phosphotyrosine
Literature citations
Subtractive hybridization reveals the expression of immunoglobulin like transcript 7, Eph-B1, granzyme B, and 3 novel transcripts in human plasmacytoid dendritic cells.
Rissoan M.-C.; Duhen T.; Bridon J.-M.; Bendriss-Vermare N.; Peronne C.; de Saint-Vis B.M.; Briere F.; Bates E.E.M.;
Blood 100:3295-3303(2002)
Cited for: NUCLEOTIDE SEQUENCE [MRNA]; FUNCTION; TISSUE SPECIFICITY; INDUCTION; VARIANT SER-294;
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]; VARIANT SER-294;
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.