Variant position: 1193 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1572 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 QNSPGTQRANARAPAPYKRD FEAKLRNFYRKLETKGYGQGP
Mouse QNSPGTQRANARAPAPYKRD FEAKLRNFYRKLETKGYGQGP
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 – 1572 E3 ubiquitin-protein ligase HECW2
1175 – 1175 Phosphoserine
214 – 1572 Missing. In isoform 2.
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
Berko E.R.; Cho M.T.; Eng C.; Shao Y.; Sweetser D.A.; Waxler J.; Robin N.H.; Brewer F.; Donkervoort S.; Mohassel P.; Boennemann C.G.; Bialer M.; Moore C.; Wolfe L.A.; Tifft C.J.; Shen Y.; Retterer K.; Millan F.; Chung W.K.;
J. Med. Genet. 54:84-86(2017)
Cited for: INVOLVEMENT IN NDHSAL; VARIANTS NDHSAL GLN-1191; VAL-1193; TRP-1330 AND GLY-1445;
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.