| Gene Symbol |
PITPNM3
|
| Entrez Gene |
83394
|
| Alt Symbol |
ACKR6, CORD5, NIR1, RDGBA3
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
PITPNM family member 3
|
| Other Description |
NIR-1|PITPnm 3|PYK2 N-terminal domain-interacting receptor 1|atypical chemokine receptor 6|cone rod dystrophy 5|membrane-associated phosphatidylinositol transfer protein 3|phosphatidylinositol transfer protein, membrane-associated 3|retinal degeneration B alpha 3
|
| Swissprots |
Q9NPQ4 F8WEW5 Q59GH9 A1A5D0 Q9BZ71
|
| Accessions |
EAW90304 EAW90305 Q9BZ71 AB209130 BAD92367 AF334586 AAK01446 AI333030 AK297617 BAH12631 AL389994 CAB97544 BC020484 BC035799 BC128583 AAI28584 BC128584 AAI28585 XM_011524014 XP_011522316 XM_011524015 XP_011522317 XM_011524016 XP_011522318 XM_011524017 XP_011522319 NM_001165966 NP_001159438 NM_031220 NP_112497
|
| Function |
Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro) (By similarity). Binds calcium ions. {ECO:0000250}.
|
| Subcellular Location |
Endomembrane system {ECO:0000305}; Peripheral membrane protein {ECO:0000305}.
|
| Tissue Specificity |
Detected in brain and spleen, and at low levels in ovary. {ECO:0000269|PubMed:10022914}.
|