| Accession | Acc. Gene-, Name | Start | End | Subsequence | Logic | PDB | Organism | Length |
|---|---|---|---|---|---|---|---|---|
| ELMI001426 | P48048 KCNJ1 IRK1_HUMAN |
216 | 222 | LIRVANLRKSLLIGSHIYGK | TP | --- | Homo sapiens (Human) | 391 |
Instance evidence
| Evidence class | PSI-MI | Method | BioSource | PubMed | Logic | Reliability | Notes |
|---|---|---|---|---|---|---|---|
| experimental | MI:0074 | mutation analysis | in vivo/in vitro | Xu,1996 | support | certain | FeatureDetection |
| experimental | MI:0424 | protein kinase assay | in vitro | Xu,1996 | support | likely | InteractionDetection |
| experimental | MI:0424 | protein kinase assay | in vivo | Xu,1996 | support | certain | InteractionDetection |
Pathways
Diseases
- Sequence Variation VAR_019726 (Pos 219) has been implicated in Bartter Syndrome, Antenatal, Type 2 (OMIM:241200).
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