| Accession | Acc. Gene-, Name | Start | End | Subsequence | Logic | PDB | Organism | Length |
|---|---|---|---|---|---|---|---|---|
| ELMI002734 | P00740 F9 FA9_HUMAN |
108 | 119 | NGGSCKDDINSYECWCPFGF | TP | --- | Homo sapiens (Human) | 461 |
Instance evidence
| Evidence class | PSI-MI | Method | BioSource | PubMed | Logic | Reliability | Notes |
|---|---|---|---|---|---|---|---|
| experimental | MI:0039 | edman degradation | in vitro | McMullen,1983 | support | likely | ParticipantIdentification |
Pathways
Diseases
- Sequence Variation VAR_006553 (Pos 113) has been implicated in Hemophilia B; Hemb (OMIM:306900).
- Sequence Variation VAR_006554 (Pos 115) has been implicated in Hemophilia B; Hemb (OMIM:306900).
- Sequence Variation VAR_006556 (Pos 119) has been implicated in Hemophilia B; Hemb (OMIM:306900).
Please cite:
The Eukaryotic Linear Motif resource: 2022 release.
(PMID:34718738)
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