Sequence information
Variant position: 176 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 201 The length of the canonical sequence.
Location on the sequence:
FIEGVQKDQMLLDTLTRSLD
L TRIVRRLQNGEQDEEGADEA
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 FIEGVQKDQMLLDTLTRSLDL TRIVRRLQNGEQDEEGAD----EA
Mouse FMEGVQKDQMLLDTLTRSLDL TGIVRRLQNGEHEEAGTGD-
Bovine FMEGVQKDQMLLDTLTRSLDL TRIVRRLQNGEQDEEGASGR
Chicken FMEGVQKDEVLLDILTRSLDL THIVKLIQNDGKNPHAPE--
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 – 201
Guanylyl cyclase-activating protein 1
Literature citations
Dysfunction of cGMP signalling in photoreceptors by a macular dystrophy-related mutation in the calcium sensor GCAP1.
Vocke F.; Weisschuh N.; Marino V.; Malfatti S.; Jacobson S.G.; Reiff C.M.; Dell'Orco D.; Koch K.W.;
Hum. Mol. Genet. 26:133-144(2017)
Cited for: VARIANT PHE-176; CHARACTERIZATION OF VARIANT PHE-176;
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.