This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
Facts about Phosphatidylinositol polyphosphate 5-phosphatase type IV.
.
Human | |
---|---|
Gene Name: | INPP5E |
Uniprot: | Q9NRR6 |
Entrez: | 56623 |
Belongs to: |
---|
inositol 1,4,5-trisphosphate 5-phosphatase type IV family |
CORS172 kDa inositol polyphosphate 5-phosphatase; CPD4; EC 3.1.3.36; inositol polyphosphate-5-phosphatase, 72 kDa; JBTS1; Joubert syndrome 1; MGC117201; MORMS; phosphatidylinositol (4,5) bisphosphate 5-phosphatase; Phosphatidylinositol polyphosphate 5-phosphatase type IV; Phosphatidylinositol-4,5-bisphosphate 5-phosphatase; PPI5PIV
Mass (kDA):
70.205 kDA
Human | |
---|---|
Location: | 9q34.3 |
Sequence: | 9; NC_000009.12 (136428619..136439861, complement) |
Detected in brain, heart, pancreas, testis and spleen.
Cytoplasm, cytoskeleton, cilium axoneme. Golgi apparatus, Golgi stack membrane; Peripheral membrane protein; Cytoplasmic side. Cell membrane; Peripheral membrane protein; Cytoplasmic side. Cell projection, ruffle. Cytoplasm. Peripheral membrane protein associated with Golgi stacks.
PMID: 10764818 by Kisseleva M.V., et al. The isolation and characterization of a cDNA encoding phospholipid- specific inositol polyphosphate 5-phosphatase.
PMID: 19668215 by Jacoby M., et al. INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse.