Sequence information
Variant position: 196 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 365 The length of the canonical sequence.
Location on the sequence:
FVRPKLVTIIRSGVKPRKAV
R VLLNKKTAHSFEQVLTDITE
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 FV---------------RPKLVTIIRSGVKPRKAVR VLLNKKTAHSFEQVLTDITE
Mouse FV---------------RPKLVTIIRSGVKPRKAVR VLLNK
Rat FV---------------RPKLVTIIRSGVKPRKAVR VLLNK
Slime mold YKESAVHSIDKFSVQTEKAKVIMCFRNGDRYHSGER VTVHS
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
1 – 365
Neuronal migration protein doublecortin
Domain
180 – 263
Doublecortin 2
Beta strand
194 – 199
Literature citations
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.
Matsumoto N.; Leventer R.J.; Kuc J.A.; Mewborn S.K.; Dudlicek L.L.; Ramocki M.B.; Pilz D.T.; Mills P.L.; Das S.; Ross M.E.; Ledbetter D.H.; Dobyns W.B.;
Eur. J. Hum. Genet. 9:5-12(2001)
Cited for: VARIANTS SBHX ARG-47; HIS-59; LEU-78; HIS-86; GLY-89; ARG-97; ALA-100; THR-104; CYS-186; TRP-192; HIS-196; ILE-200; LYS-200; ALA-203; ARG-203; THR-214; VAL-223 AND SER-251;
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.
Demelas L.; Serra G.; Conti M.; Achene A.; Mastropaolo C.; Matsumoto N.; Dudlicek L.L.; Mills P.L.; Dobyns W.B.; Ledbetter D.H.; Das S.;
Neurology 57:327-330(2001)
Cited for: VARIANT LISX1 HIS-196;
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.