SYTL1 - synaptotagmin like 1 Gene
Also Known as JFC1; SLP1
Species: Homo sapiens
About SYTL1
This gene has 11 transcripts (splice variants), 176 orthologues and 31 paralogues. Broad expression in prostate (RPKM 24.6), skin (RPKM 21.7) and 16 other tissues.
Summary
Predicted to enable neurexin family protein binding activity. Involved in exocytosis. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]
SYTL1 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001193308.2 | NP_001180237.1 | synaptotagmin-like protein 1 isoform 1 |
| NM_032872.3 | NP_116261.1 | synaptotagmin-like protein 1 isoform 2 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
18266782 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in exocytosis |
IDA
IDA: Inferred from direct assay
|
18266782 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in plasma membrane |
IDA
IDA: Inferred from direct assay
|
18266782 | GOA |
SYTL1 Protein Structure
C2: C2 domain (283 - 367)
C2: C2 domain (424 - 509)
- 0
- 100
- 200
- 300
- 400
- 500
- 562 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
synaptotagmin-like protein 1 |
|
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Severe Congenital Neutropenia 7 |
|
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| Joubert Syndrome 30 |
|
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| Bladder Cancer |
|
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