Sequence information
Variant position: 280 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 323 The length of the canonical sequence.
Location on the sequence:
FPSANLRGRHPGGERTCPSW
V VVLYRKNRSLAAPRGPGLVK
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 FPSANLRGR--HPGGE--RTCPSWV VVLYRKNRS-------LAAPRGPGLVK
Mouse ---ANKRFV--FHNEQ--VYCPDCA KKL-------------
Rat ---ANKRFV--FHNEQ--VYCPDCA KKL-------------
Baker's yeast SASASSHPNNYLHDKQPGSFDPSSL SRFFQPRQNARATSSV
Fission yeast SISVTQRPA--VNVGPPPYVRPSAP SKLPDTRQS-------
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
2 – 323
Four and a half LIM domains protein 1
Alternative sequence
168 – 296
Missing. In isoform 3.
Alternative sequence
231 – 323
KRTVSRVSHPVSKARKPPVCHGKRLPLTLFPSANLRGRHPGGERTCPSWVVVLYRKNRSLAAPRGPGLVKAPVWWPMKDNPGTTTASTAKNAP -> FGKGSSVVAYEGQSWHDYCFHCKKCSVNLANKRFVFHQEQVYCPDCAKKL. In isoform 1, isoform 4 and isoform 5.
Literature citations
Consequences of mutations within the C terminus of the FHL1 gene.
Schoser B.; Goebel H.H.; Janisch I.; Quasthoff S.; Rother J.; Bergmann M.; Mueller-Felber W.; Windpassinger C.;
Neurology 73:543-551(2009)
Cited for: VARIANTS XMPMA TRP-224 AND MET-280; VARIANT XMPMA TYR-246 (ISOFORM 1); VARIANT ASN-275 (ISOFORM 1);
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.