RBM10
Summary: This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011].
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Name | OMIM ID | Ensembl ID | HGNC ID | PHARMGKB ID | Map Location |
|---|---|---|---|---|---|
OMIM IDMIM:300080 Ensembl IDEnsembl:ENSG00000182872 HGNC IDHGNC:HGNC:9896 PHARMGKB IDPA34259 Map LocationXp11.3 | |||||
GO terms in RBM10
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Term Type | Evidence Type | GO Term ID | GO Des. |
|---|---|---|---|
| CC | IDA | GO:0005634 | nucleus |
| CC | IDA | GO:0016607 | nuclear speck |
| BP | IEA | GO:0000381 | regulation of alternative mRNA splicing, via spliceosome |
| BP | IEA | GO:0006397 | mRNA processing |
| BP | ND | GO:0008150 | biological_process |
| BP | IEA | GO:0008380 | RNA splicing |
Gene expression in normal tissue: RBM10
Gene-model tissue-cancer distribution: Bubble Plot
Gene-drug pathway distribution
Pathways in RBM10
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Database | Pathway ID | Pathway Des. |
|---|---|---|
| No matching records found | ||
Gene-Drug: Aster Plot
Gene in drug-gene network: Network Plot
Gene-drug targets distribution
Gene Structure: PDB
Models in RBM10
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Model | Level | Reference ID | Tissue | Cancer | Drug | Clinical Response | Source | |
|---|---|---|---|---|---|---|---|---|
| No matching records found | ||||||||
CLASSFICATION
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