Accession | Acc. Gene-, Name | Start | End | Subsequence | Logic | PDB | Organism | Length |
---|---|---|---|---|---|---|---|---|
ELMI002168 | P51168 SCNN1B SCNNB_HUMAN |
617 | 620 | ALPIPGTPPPNYDSLRLQPL | TP | --- | Homo sapiens (Human) | 640 |
Instance evidence
Evidence class | PSI-MI | Method | BioSource | PubMed | Logic | Reliability | Notes |
---|---|---|---|---|---|---|---|
experimental | MI:0007 | anti tag coimmunoprecipitation | in vivo | Zhou,2007 | support | certain | InteractionDetection |
experimental | MI:0256 | rna interference | in vivo | Zhou,2007 | support | certain | InteractionDetection |
experimental | MI:0997 | ubiquitinase assay | in vitro | Zhou,2007 | support | certain | InteractionDetection |
experimental | MI:0074 | mutation analysis | in vivo/in vitro | Zhou,2007 | support | certain | FeatureDetection |
experimental | MI:0113 | western blot | in vitro | Zhou,2007 | support | certain | ParticipantIdentification FeatureDetection |
Pathways
KEGG: The sequence P51168 is implicated in the following 2 Pathways: (color codes: This sequence=red, interacting sequence=orange)Diseases
- Sequence Variation VAR_026522 (Pos 620) has been implicated in Liddle Syndrome; Lidls (OMIM:177200).
- Sequence Variation VAR_026521 (Pos 618) has been implicated in Liddle Syndrome; Lidls (OMIM:177200).
- Sequence Variation VAR_026520 (Pos 617) has been implicated in Liddle Syndrome; Lidls (OMIM:177200).
Please cite:
ELM-the Eukaryotic Linear Motif resource-2024 update.
(PMID:37962385)
ELM data can be downloaded & distributed for non-commercial use according to the ELM Software License Agreement
ELM data can be downloaded & distributed for non-commercial use according to the ELM Software License Agreement