Variant position: 215 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 376 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 LQSGFLNNSWPLPQPPSPMP YASCQMAAAAAAAAAAAAAAG
Mouse LQSGFLNNSWPLPQPPSPMP YASCQMAAAAAAAAAAAAAAG
Pig LQSGFLNNSWPLPQPPSPMP YASCQMAAAAAAAAAAAAAAG
Bovine LQSGFLNNSWPLPQPPSPMP YASCQMAAAAAAAAAAAAAAG
Rabbit LQSGFLNNSWPLPQPPSPMP YASCQMAAAAAAAAAAAAAAG
Goat LQSGFLNNSWPLPQPPSPMP YASCQMAAAAAAAAAAAAAAG
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
1 – 376 Forkhead box protein L2
Genetic analysis of a five generation Indian family with BPES: a novel missense mutation (p.Y215C).
Kumar A.; Babu M.; Raghunath A.; Venkatesh C.P.;
Mol. Vis. 10:445-449(2004)
Cited for: VARIANT BPES CYS-215;
Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients.
Nallathambi J.; Laissue P.; Batista F.; Benayoun B.A.; Lesaffre C.; Moumne L.; Pandaranayaka P.E.; Usha K.; Krishnaswamy S.; Sundaresan P.; Veitia R.A.;
Hum. Mutat. 29:E123-E131(2008)
Cited for: VARIANTS BPES ARG-98; PRO-108; CYS-215; CYS-217 AND ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-ALA-234 INS; VARIANT GLY-179; CHARACTERIZATION OF VARIANTS BPES PRO-108 AND CYS-217;
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.