Variant position: 42 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 615 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 LFAAELGREEPDLVLLSLVL GFVEHFLAVNRVIPTNVPELT
Mouse LFAAELGREEPDLVLLSLVL GFVEHFLAVNRVIPTNVPELT
Rat LFAAELGREEPDLVLLSLVL GFVEHFLAVNRVIPTNVPELT
Bovine LFAAELGREEPDLVLLSLVL GFVEHFLAVNRVIPTNVPELT
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.
Characterization of mutations in patients with multiple endocrine neoplasia type 1.
Bassett J.H.D.; Forbes S.A.; Pannett A.A.J.; Lloyd S.E.; Christie P.T.; Wooding C.; Harding B.; Besser G.M.; Edwards C.R.; Monson J.P.; Sampson J.; Wass J.A.H.; Wheeler M.H.; Thakker R.V.;
Am. J. Hum. Genet. 62:232-244(1998)
Cited for: VARIANTS MEN1 ASP-42; PRO-165; ASP-169; SER-188 AND GLU-289;
Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein.
Wautot V.; Vercherat C.; Lespinasse J.; Chambe B.; Lenoir G.M.; Zhang C.X.; Porchet N.; Cordier M.; Beroud C.; Calender A.;
Hum. Mutat. 20:35-47(2002)
Cited for: VARIANTS MEN1 TRP-39; ASP-42; LEU-98; PRO-165; THR-165; PHE-167; ASP-169; ARG-170; TYR-177; PRO-228; PHE-245; ARG-286; PRO-316; PRO-319; TYR-322; ARG-322; ASP-342; ARG-346; HIS-362; ASP-373; MET-377; ASN-423; CYS-532; ASN-560 AND ARG-560;
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.