SNX10 - sorting nexin 10 Gene
Also Known as OPTB8
Species: Homo sapiens
About SNX10
This gene has 27 transcripts (splice variants), 278 orthologues, 15 paralogues and is associated with 2 phenotypes. Broad expression in brain (RPKM 20.5), appendix (RPKM 13.4) and 19 other tissues.
Summary
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. This gene may play a role in regulating endosome homeostasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]
SNX10 Products (8)
| mRNA | Protein | Name |
|---|---|---|
| NM_001199835.1 | NP_001186764.1 | sorting nexin-10 isoform 1 |
| NM_001199837.3 | NP_001186766.1 | sorting nexin-10 isoform 2 |
| NM_001199838.2 | NP_001186767.1 | sorting nexin-10 isoform 3 |
| NM_001318198.1 | NP_001305127.1 | sorting nexin-10 isoform 4 |
| NM_001318199.3 | NP_001305128.1 | sorting nexin-10 isoform 1 |
| NM_001362753.1 | NP_001349682.1 | sorting nexin-10 isoform 4 |
| NM_001362754.1 | NP_001349683.1 | sorting nexin-10 isoform 4 |
| NM_013322.3 | NP_037454.2 | sorting nexin-10 isoform 1 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables 1-phosphatidylinositol binding |
IMP
IMP: Inferred from mutant phenotype
|
17012226 | GOA |
| enables ATPase binding |
IPI
IPI: Inferred from physical interaction
|
21844891 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
25416956 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in cilium assembly |
IMP
IMP: Inferred from mutant phenotype
|
21844891 | GOA |
| involved in endosome organization |
IMP
IMP: Inferred from mutant phenotype
|
17012226 | GOA |
| involved in protein localization to centrosome |
IMP
IMP: Inferred from mutant phenotype
|
21844891 | GOA |
| involved in protein localization to cilium |
IMP
IMP: Inferred from mutant phenotype
|
21844891 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| colocalizes with centrosome |
IDA
IDA: Inferred from direct assay
|
21844891 | GOA |
| located in endoplasmic reticulum |
IDA
IDA: Inferred from direct assay
|
22174188 | GOA |
| located in extrinsic component of endosome membrane |
IDA
IDA: Inferred from direct assay
|
17012226 | GOA |
| located in nucleus |
IDA
IDA: Inferred from direct assay
|
22174188 | GOA |
SNX10 Protein Structure
PX: PX domain (12 - 123)
- 0
- 100
- 201 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
sorting nexin-10 |
|
SNX10 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
SNX10 | Q9Y5X0 | PRKCA | Homo sapiens | P17252 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | PRKCA | Homo sapiens | P17252 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | PRKCA | Homo sapiens | P17252 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | YIF1A | Homo sapiens | O95070 | 32296183 | |
|
Intra
|
SNX10 | Q9Y5X0 | YIF1A | Homo sapiens | O95070 | 32296183 | |
|
Intra
|
SNX10 | Q9Y5X0 | YWHAG | Homo sapiens | P61981 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | YWHAG | Homo sapiens | P61981 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | YWHAG | Homo sapiens | P61981 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | KAT5 | Homo sapiens | Q92993 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | KAT5 | Homo sapiens | Q92993 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | KAT5 | Homo sapiens | Q92993 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | RABAC1 | Homo sapiens | Q9UI14 | 32296183 | |
|
Intra
|
SNX10 | Q9Y5X0 | RABAC1 | Homo sapiens | Q9UI14 | 32296183 | |
|
Intra
|
SNX10 | Q9Y5X0 | ARL6IP1 | Homo sapiens | Q15041 | 32296183 | |
|
Intra
|
SNX10 | Q9Y5X0 | ARL6IP1 | Homo sapiens | Q15041 | 32296183 | |
|
Intra
|
SNX10 | Q9Y5X0 | ARL6IP1 | Homo sapiens | Q15041 | 25416956 | |
|
Intra
|
SNX10 | Q9Y5X0 | SETDB1 | Homo sapiens | Q15047-2 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | SETDB1 | Homo sapiens | Q15047-2 | 32814053 | |
|
Intra
|
SNX10 | Q9Y5X0 | SETDB1 | Homo sapiens | Q15047-2 | 32814053 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Osteopetrosis, Autosomal Recessive 8 |
|
|
| Autosomal Recessive Malignant Osteopetrosis |
|
|
| Osteopetrosis |
|
|
| Osteopetrosis, Autosomal Recessive 2 |
|
|
| Pycnodysostosis |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Macaca mulatta | SNX10 | VGNC | VGNC:77705 |
| Bos taurus | SNX10 | VGNC | VGNC:35091 |
| Mus musculus | SNX10 | MGD | MGI:1919232 |
| Felis catus | SNX10 | VGNC | VGNC:102706 |
| Rattus norvegicus | SNX10 | RGD | RGD:1305782 |
| Canis familiaris | SNX10 | VGNC | VGNC:46620 |
| Others | SNX10 | NCBI |