Basic information
- Full name
- inositol polyphosphate-5-phosphatase D
- Ensembl
- ENSG00000168918.14
- Summary
- This gene is a member of the inositol polyphosphate-5-phosphatase (INPP5) family and encodes a protein with an N-terminal SH2 domain, an inositol phosphatase domain, and two C-terminal protein interaction domains. Expression of this protein is restricted to hematopoietic cells where its movement from the cytosol to the plasma membrane is mediated by tyrosine phosphorylation. At the plasma membrane, the protein hydrolyzes the 5' phosphate from phosphatidylinositol (3,4,5)-trisphosphate and inositol-1,3,4,5-tetrakisphosphate, thereby affecting multiple signaling pathways. The protein is also partly localized to the nucleus, where it may be involved in nuclear inositol phosphate signaling processes. Overall, the protein functions as a negative regulator of myeloid cell proliferation and survival. Mutations in this gene are associated with defects and cancers of the immune system. Deficiencies in the encoded protein, SHIP1, have been associated with Inflammatory Bowel Disease types such as Crohn's Disease and Ulcerative Colitis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2020]
- Annotation
- Druggable target (Tier T3) Phosphatase
Protein product
- ENST00000445964.6 Primary ENSP00000405338.2 (38 phosphosites)
- ENST00000359570.9
Phosphosites on the primary protein product
Tumor and normal comparison
Signed p-values | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Data type | Meta P | BRCA | CCRCC | COAD | GBM | HNSCC | LSCC | LUAD | OV | PDAC | UCEC |
RNA | 4.7e-3 | - | 1.9e-27 | - | - | -0.49 | -1.2e-11 | -8.4e-7 | - | -0.033 | - |
protein | 1.4e-17 | - | 2.5e-26 | 1.1e-12 | - | 2.3e-5 | -0.021 | -0.95 | -0.85 | 1.4e-4 | 0.35 |
mRNA expression at gene level
Protein expression
Phenotype and mutation association
Manhattan plot summarizing associations of phenotypes and mutations across all cohorts and omics data types
Associations of the protein abundance of INPP5D with phenotypes and mutations
Signed p-values | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Phenotype | Meta P | BRCA | CCRCC | COAD | GBM | HNSCC | LSCC | LUAD | OV | PDAC | UCEC | |
ESTIMATE: ImmuneScore | 4.9e-123 | 2.2e-16 | 2.2e-16 | 0.47 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | |
HALLMARK_ALLOGRAFT_REJECTION | 7.1e-123 | 2.2e-16 | 2.2e-16 | 0.5 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | |
xcell: immune score | 1.1e-116 | 2.2e-16 | 2.2e-16 | 0.28 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 4.4e-9 | 2.2e-16 | |
ESTIMATE: ESTIMATEScore | 3.0e-109 | 2.2e-16 | 2.2e-16 | 0.44 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 1.8e-9 | 2.2e-16 | 2.4e-9 | 2.2e-16 | |
xcell: microenvironment score | 2.7e-106 | 2.2e-16 | 2.2e-16 | 0.24 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 1.3e-7 | 9.6e-8 | |
HALLMARK_COMPLEMENT | 2.2e-105 | 2.2e-16 | 2.2e-16 | 0.97 | 2.2e-16 | 1.6e-20 | 2.2e-16 | 3.1e-6 | 2.2e-16 | 1.2e-8 | 2.2e-16 | |
HALLMARK_IL6_JAK_STAT3_SIGNALING | 2.2e-101 | 2.2e-16 | 2.2e-16 | -0.75 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 3.9e-8 | 2.2e-16 | 6.7e-7 | 2.2e-16 | |
HALLMARK_INFLAMMATORY_RESPONSE | 3.9e-96 | 2.2e-16 | 2.2e-16 | -0.27 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 1.1e-6 | 2.2e-16 | 5.1e-6 | 2.2e-16 | |
HALLMARK_IL2_STAT5_SIGNALING | 1.4e-92 | 2.2e-16 | 2.8e-8 | 0.89 | 2.2e-16 | 2.2e-16 | 2.2e-16 | 1.5e-8 | 2.2e-16 | 8.5e-5 | 2.2e-16 | |
HALLMARK_INTERFERON_GAMMA_RESPONSE | 2e-83 | 2.2e-16 | 2.2e-16 | -0.95 | 8.7e-9 | 2.2e-16 | 2.2e-16 | 7.4e-6 | 5.3e-9 | 3.5e-5 | 2.2e-16 |
Cis-association
Associations between omics data of INPP5D
Trans-association
Associations of the protein abundance of INPP5D and the protein abundance of other genes
Signed p-values | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Gene | Meta P | BRCA | CCRCC | COAD | GBM | HNSCC | LSCC | LUAD | OV | PDAC | UCEC | |
No matching records found |
Gene set enrichment analysis
Submit genes and the common logarithm of the p-values of their association with to WebGestalt.