WormBase Tree Display for Gene: HGNC:11506
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HGNC:11506 | Identity | Name | CGC_name | Syp | Inferred_automatically | AGR_import |
---|---|---|---|---|---|---|
Other_name | RGD:737494 | |||||
MRX96 | ||||||
MRXSYP | ||||||
XLID96 | ||||||
major synaptic vesicle protein P38 | ||||||
Public_name | Syp | |||||
DB_info | Database | HGNC | id | 11506 | ||
AGR | cURI | HGNC:11506 | ||||
EnsEMBL | ENSEMBL_geneID | ENSG00000102003 | ||||
UniProt | UniProt_AC | P08247 | ||||
OMIM | gene | 313475 | ||||
DO | id | DOID:10652 | ||||
DOID:0112035 | ||||||
Species | Homo sapiens | |||||
Status | Live | |||||
Gene_info | Biotype | SO:0001217 | ||||
Ortholog | WBGene00004979 | Caenorhabditis elegans | From_analysis | Hieranoid | ||
Inparanoid | ||||||
OMA | ||||||
OrthoFinder | ||||||
OrthoInspector | ||||||
Panther | ||||||
Structured_description | Automated_description | This gene encodes an integral membrane protein of small synaptic vesicles in brain and endocrine cells. The protein also binds cholesterol and is thought to direct targeting of vesicle-associated membrane protein 2 (synaptobrevin) to intracellular compartments. Mutations in this gene are associated with an X-linked form of cognitive disability. [provided by RefSeq, Jul 2017] | Inferred_automatically | AGR_import |