Variant position: 153 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 911 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 EIVDGNAKMTLGMIWTIILR FAIQDISVEETSAKEGLLLWC
Mouse EIVDGNAKMTLGMIWTIILR FAIQDISVEETSAKEGLLLWC
Rat EIVDGNAKMTLGMIWTIILR FAIQDISVEETSAKEGLLLWC
Bovine EIVDGNAKMTLGMIWTIILR FAIQDISVEETSAKEGLLLWC
Chicken EIVDGNAKMTLGMIWTIILR FAIQDISVEETSAKEGLLLWC
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 – 911 Alpha-actinin-4
50 – 154 Calponin-homology (CH) 1
1 – 269 Actin-binding
54 – 272 Missing. In isoform ACTN4ISO.
89 – 478 Missing. In isoform 3.
139 – 154
Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis.
Barua M.; Brown E.J.; Charoonratana V.T.; Genovese G.; Sun H.; Pollak M.R.;
Kidney Int. 83:316-322(2013)
Cited for: VARIANTS FSGS1 ARG-59; GLN-72; LEU-153; GLU-255; ILE-259 AND PRO-262;
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.