Variant position: 142 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 213 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 SSEELQANKATLVCLMNDFY PGILTVTWKADGTPITQGVEM
Mouse SLKNLQANKATLVCLVSEFY PGTLVVDWKVDGVPVTQGVET
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
38 – 213 Immunoglobulin lambda-like polypeptide 1
114 – 208 Ig-like C1-type
109 – 213 C region (By similarity to lambda light-chain)
135 – 194
70 – 213 FLLQRGSWTGPRCWPRGFQSKHNSVTHVFGSGTQLTVLSQPKATPSVTLFPPSSEELQANKATLVCLMNDFYPGILTVTWKADGTPITQGVEMTTPSKQSNNKYAASSYLSLTPEQWRSRRSYSCQVMHEGSTVEKTVAPAECS -> SAQGHPLGHSVPAVL. In isoform 2.
131 – 143
Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemia.
Minegishi Y.; Coustan-Smith E.; Wang Y.H.; Cooper M.D.; Campana D.; Conley M.E.;
J. Exp. Med. 187:71-77(1998)
Cited for: FUNCTION; SUBCELLULAR LOCATION; VARIANT AGM2 LEU-142;
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.