Variant position: 697 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 902 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 TKEFFRRSKIAVYEKMWTYM RSAEPSVFTRTTAEGVARVRK
Mouse TKEFFRRSKIAVYEKMWTYM RSAEPSVFTRTTAEGVARVRK
Rat TKEFFRRSKIAVYEKMWTYM RSAEPSVFTRTTAEGVARVRK
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
21 – 902 Glutamate receptor 4
639 – 813 Extracellular
434 – 902 Missing. In isoform 2.
De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait Abnormalities.
Martin S.; Chamberlin A.; Shinde D.N.; Hempel M.; Strom T.M.; Schreiber A.; Johannsen J.; Ousager L.B.; Larsen M.J.; Hansen L.K.; Fatemi A.; Cohen J.S.; Lemke J.; Soerensen K.P.; Helbig K.L.; Lessel D.; Abou Jamra R.;
Am. J. Hum. Genet. 101:1013-1020(2017)
Cited for: INVOLVEMENT IN NEDSGA; VARIANTS NEDSGA SER-639; ASP-641; GLY-643; VAL-644 AND PRO-697;
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.