Variant position: 184 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 860 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 LWACDNDPDCEDGSDEWPQR CRGLYVFQ--GDSSPCSAFEFHC
Mouse LWACDGDVDCVDGSDEWPQN CQGRDTASK-GVSSPCSSLEF
Rat LWACDGDRDCDDGSDEWPQN CGAEDTAAE-VVSSPCSSLEF
Bovine LWACDGDPDCDDGSDEWPKH CGTPHPSGPLQDNNPCSALEF
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
22 – 860 Low-density lipoprotein receptor
22 – 788 Extracellular
146 – 186 LDL-receptor class A 4
167 – 184
105 – 272 Missing. In isoform 3.
106 – 232 Missing. In isoform 2.
Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of Scotland.
Lee W.K.; Haddad L.; Macleod M.J.; Dorrance A.M.; Wilson D.J.; Gaffney D.; Dominiczak M.H.; Packard C.J.; Day I.N.; Humphries S.E.; Dominiczak A.F.;
J. Med. Genet. 35:573-578(1998)
Cited for: VARIANT FHCL1 GLASCO TYR-184;
Presence and type of low density lipoprotein receptor (LDLR) mutation influences the lipid profile and response to lipid-lowering therapy in Brazilian patients with heterozygous familial hypercholesterolemia.
Santos P.C.; Morgan A.C.; Jannes C.E.; Turolla L.; Krieger J.E.; Santos R.D.; Pereira A.C.;
Cited for: VARIANTS FHCL1 TYR-160; ALA-168; LEU-177; TYR-184; GLY-221; GLN-228; LYS-228; TRP-276; TYR-285; GLY-301; PHE-318; CYS-326; SER-343; TYR-368; ASP-373; TRP-406; MET-429; ASN-492; ASP-549; HIS-564; HIS-574; TRP-595; HIS-601; LEU-685; LEU-699; MET-797 AND GLN-814;
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.