MYRIP - myosin VIIA and Rab interacting protein Gene
Also Known as SLAC2C; SLAC2-C
Species: Homo sapiens
About MYRIP
This gene has 10 transcripts (splice variants), 116 orthologues and 2 paralogues. Broad expression in brain (RPKM 7.4), spleen (RPKM 4.2) and 23 other tissues.
Summary
Predicted to enable actin binding activity and Myosin binding activity. Predicted to be involved in positive regulation of Insulin secretion. Predicted to be located in actin cytoskeleton; dense core granule; and perinuclear region of cytoplasm. Predicted to be part of exocyst. Predicted to be active in cortical actin Cytoskeleton. [provided by Alliance of Genome Resources, Apr 2022]
MYRIP Products (5)
| mRNA | Protein | Name |
|---|---|---|
| NM_001284423.2 | NP_001271352.1 | rab effector MyRIP isoform a |
| NM_001284424.2 | NP_001271353.1 | rab effector MyRIP isoform b |
| NM_001284425.2 | NP_001271354.1 | rab effector MyRIP isoform c |
| NM_001284426.2 | NP_001271355.1 | rab effector MyRIP isoform d |
| NM_015460.4 | NP_056275.2 | rab effector MyRIP isoform a |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
11964381 | GOA |
MYRIP Protein Structure
FYVE_2: FYVE-type zinc finger (9 - 125)
Rab_eff_C: Rab effector MyRIP/melanophilin C-terminus (152 - 859)
- 0
- 200
- 400
- 600
- 800
- 859 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
rab effector MyRIP |
|
MYRIP Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
MYRIP | Q8NFW9 | OIP5 | Homo sapiens | O43482 | 32296183 | |
|
Intra
|
MYRIP | Q8NFW9 | OIP5 | Homo sapiens | O43482 | 32296183 | |
|
Intra
|
MYRIP | Q8NFW9 | C1orf216 | Homo sapiens | Q8TAB5 | 32296183 | |
|
Intra
|
MYRIP | Q8NFW9 | C1orf216 | Homo sapiens | Q8TAB5 | 25416956 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Deafness, Autosomal Dominant 50 |
|
|
| Griscelli Syndrome |
|
|
| Cerebrooculofacioskeletal Syndrome 1 |
|
|
| Usher Syndrome |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Mus musculus | MYRIP | MGD | MGI:2384407 |
| Felis catus | MYRIP | VGNC | VGNC:102783 |
| Bos taurus | MYRIP | VGNC | VGNC:31846 |
| Macaca mulatta | MYRIP | VGNC | VGNC:74992 |
| Rattus norvegicus | MYRIP | RGD | RGD:727731 |
| Canis familiaris | MYRIP | VGNC | VGNC:43589 |
| Others | MYRIP | NCBI |