SHISA5 - shisa family member 5 Gene
Also Known as SCOTIN
Species: Homo sapiens
About SHISA5
This gene has 19 transcripts (splice variants), 121 orthologues and 2 paralogues. Ubiquitous expression in placenta (RPKM 49.3), spleen (RPKM 32.3) and 25 other tissues.
Summary
This gene encodes a member of the shisa family. The encoded protein is localized to the endoplasmic reticulum, and together with p53 induces Apoptosis in a caspase-dependent manner. Alternative splicing results in multiple transcript variants. Related pseudogenes of this gene are found on chromosome X. [provided by RefSeq, Apr 2016]
SHISA5 Products (7)
| mRNA | Protein | Name |
|---|---|---|
| NM_001272065.3 | NP_001258994.1 | protein shisa-5 isoform b precursor |
| NM_001272066.2 | NP_001258995.1 | protein shisa-5 isoform c |
| NM_001272067.2 | NP_001258996.1 | protein shisa-5 isoform c |
| NM_001272068.2 | NP_001258997.1 | protein shisa-5 isoform c |
| NM_001272082.4 | NP_001259011.1 | protein shisa-5 isoform d |
| NM_001272083.4 | NP_001259012.1 | protein shisa-5 isoform e |
| NM_016479.6 | NP_057563.3 | protein shisa-5 isoform a precursor |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables WW domain binding |
IPI
IPI: Inferred from physical interaction
|
15064722 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
15064722 | GOA |
SHISA5 Protein Structure
Shisa: Wnt and FGF inhibitory regulator (27 - 209)
- 0
- 100
- 200
- 240 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
protein shisa-5 |
|
SHISA5 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Cross
|
SHISA5 | Q8N114 | Pdcd6 | Mus musculus | P12815 | 17889823 | |
|
Cross
|
SHISA5 | Q8N114 | Pdcd6 | Mus musculus | P12815 | 17889823 | |
|
Cross
|
SHISA5 | Q8N114 | Pdcd6 | Mus musculus | P12815 | 17889823 | |
|
Intra
|
SHISA5 | Q8N114 | WWOX | Homo sapiens | Q9NZC7 | 15064722 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Bn2 Diffuse Large B-Cell Lymphoma |
|
|
| Microcephaly 6, Primary, Autosomal Recessive |
|
|
| Fanconi Anemia, Complementation Group C |
|
|