The Eukaryotic Linear Motif resource for
Functional Sites in Proteins

o  Instance

Accession Acc. Gene-, NameStartEndSubsequenceLogic PDB OrganismLength
ELMI000553 P41180 CASR
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  Pathways

KEGG: The sequence P41180 is implicated in the following 2 Pathways: (color codes: This sequence=red, interacting sequence=orange)

o  Diseases

  • Sequence Variation VAR_058054 (Pos 131) has been implicated in Hypocalcemia, Autosomal Dominant 1; Hypoc1 (OMIM:601198).
Please cite: The Eukaryotic Linear Motif resource: 2022 release. (PMID:34718738)

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