The Eukaryotic Linear Motif resource for
Functional Sites in Proteins

o  Instance

Accession Acc. Gene-, NameStartEndSubsequenceLogic PDB OrganismLength
ELMI000553 P41180 CASR
CASR_HUMAN
129 134 SLNLDEFCNCSEHIPSTIAV TP --- Homo sapiens (Human) 1078

o  Instance evidence

Evidence classPSI-MIMethodBioSourcePubMedLogicReliabilityNotes
not annotated not specified Ray,1998 not specified not specified

o  Diseases

  • Sequence Variation VAR_058054 (Pos 131) has been implicated in Hypocalcemia, Autosomal Dominant 1; Hypoc1 (OMIM:601198).
Please cite: ELM 2016-data update and new functionality of the eukaryotic linear motif resource. (PMID:26615199)

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