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- Table of Contents
Facts about Membrane-associated phosphatidylinositol transfer protein 3.
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Human | |
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Gene Name: | PITPNM3 |
Uniprot: | Q9BZ71 |
Entrez: | 83394 |
Belongs to: |
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PtdIns transfer protein family |
membrane-associated phosphatidylinositol transfer protein 3; MGC157740; MGC157741; NIR-1; NIR1CORD5; Phosphatidylinositol transfer protein, membrane-associated 3; PITPnm 3; PITPNM family member 3; Pyk2 N-terminal domain-interacting receptor 1; RDGBA3; retinal degeneration B alpha 3
Mass (kDA):
106.781 kDA
Human | |
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Location: | 17p13.2-p13.1 |
Sequence: | 17; NC_000017.11 (6451263..6556555, complement) |
Detected in brain and spleen, and at low levels in ovary.
Endomembrane system; Peripheral membrane protein.
PMID: 10022914 by Lev S., et al. Identification of a novel family of targets of PYK2 related to Drosophila retinal degeneration B (rdgB) protein.
PMID: 17377520 by Koehn L., et al. Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.