Variant position: 756 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 863 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 ALYYKKDKRRHDVHRRCSPQ RTTTNDLTHAQEEEIMSLQMK
Mouse ALYYKKDKRRHDVHRRCSPQ RTTTNDLTHAPEEEIMSLQMK
Rat ALYYKKDKRRHDVHRRCSPQ RTTTNDLTHAPEEEIMSLQMK
Caenorhabditis elegans AVRREWGKKRRN-------- ------------EKKFQLQYQ
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
46 – 863 Neuroligin-1
739 – 863 Cytoplasmic
Functional significance of rare neuroligin 1 variants found in autism.
Nakanishi M.; Nomura J.; Ji X.; Tamada K.; Arai T.; Takahashi E.; Bucan M.; Takumi T.;
PLoS Genet. 13:e1006940-e1006940(2017)
Cited for: FUNCTION; SUBCELLULAR LOCATION; TISSUE SPECIFICITY; VARIANTS AUTS20 LEU-89; ILE-90; PRO-309; GLU-337 AND TYR-835; VARIANT HIS-756; CHARACTERIZATION OF VARIANTS AUTS20 LEU-89; ILE-90; PRO-309; GLU-337 AND TYR-835; CHARACTERIZATION OF VARIANT HIS-756;
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.