EXOC6B - exocyst complex component 6B Gene
Also Known as SEC15B; SEC15L2; SEMDJL3
Species: Homo sapiens
About EXOC6B
This gene has 9 transcripts (splice variants), 219 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in heart (RPKM 12.8), brain (RPKM 8.7) and 23 other tissues.
Summary
This gene encodes a protein which is a part of the evolutionarily conserved exocyst, a multimeric protein complex necessary for exocytosis, which in turn, is crucial for cell growth, polarity and migration. Disruption of this gene may be associated with phenotypes exhibiting multiple symptoms including intellectual disability and developmental delay (DD). [provided by RefSeq, Jun 2016]
EXOC6B Products (6)
| mRNA | Protein | Name |
|---|---|---|
| NM_001321729.2 | NP_001308658.1 | exocyst complex component 6B isoform 1 |
| NM_001321730.2 | NP_001308659.1 | exocyst complex component 6B isoform 3 |
| NM_001321731.2 | NP_001308660.1 | exocyst complex component 6B isoform 4 |
| NM_001321733.2 | NP_001308662.1 | exocyst complex component 6B isoform 5 |
| NM_001321734.2 | NP_001308663.1 | exocyst complex component 6B isoform 6 |
| NM_015189.3 | NP_056004.1 | exocyst complex component 6B isoform 2 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
27173435 | GOA |
EXOC6B Protein Structure
Sec15: Exocyst complex subunit Sec15-like (465 - 772)
- 0
- 200
- 400
- 600
- 811 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
exocyst complex component 6B |
|
EXOC6B Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
EXOC6B | Q9Y2D4 | SHTN1 | Homo sapiens | A0MZ66-4 | 32296183 | |
|
Intra
|
EXOC6B | Q9Y2D4 | SHTN1 | Homo sapiens | A0MZ66-4 | 32296183 | |
|
Intra
|
EXOC6B | Q9Y2D4 | EXOC5 | Homo sapiens | O00471 | 33961781 | |
|
Intra
|
EXOC6B | Q9Y2D4 | EXOC5 | Homo sapiens | O00471 | 27173435 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 |
|
|
| Spondyloepimetaphyseal Dysplasia With Joint Laxity |
|
|
| Spondyloepimetaphyseal Dysplasia |
|
|
| Spondyloepimetaphyseal Dysplasia, X-Linked |
|
|
| Laurin-Sandrow Syndrome |
|
|
| Scoliosis |
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Felis catus | EXOC6B | VGNC | VGNC:62003 |
| Rattus norvegicus | EXOC6B | RGD | RGD:1560638 |
| Macaca mulatta | EXOC6B | VGNC | VGNC:106160 |
| Bos taurus | EXOC6B | VGNC | VGNC:28651 |
| Canis familiaris | EXOC6B | VGNC | VGNC:40517 |
| Mus musculus | EXOC6B | MGD | MGI:1923164 |
| Others | EXOC6B | NCBI |