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- Table of Contents
Facts about Noelin-2.
Plays a role in AMPAR complex organization (By similarity). Is a regulator of vascular smooth-muscle cell (SMC) phenotypic switching, that acts by promoting RUNX2 and inhibiting MYOCD binding to SRF.
| Human | |
|---|---|
| Gene Name: | OLFM2 |
| Uniprot: | O95897 |
| Entrez: | 93145 |

| Belongs to: |
|---|
| No superfamily |

neuronal olfactomedin related ER localized protein 2; NOE2; NOE2noelin 2; NOELIN2; Noelin-2; NOELIN2_V1; olfactomedin 2; Olfactomedin2; Olfactomedin-2; OlfC; OLFM2; OM2
Mass (kDA):
51.386 kDA

| Human | |
|---|---|
| Location: | 19p13.2 |
| Sequence: | 19; NC_000019.10 (9853718..9936515, complement) |
Expressed in aortic smooth muscle (at protein level) (PubMed:25298399). In the fetus, expressed in the brain and ocular tissues including lens vesicle and optic cup (PubMed:27844144).
Secreted. Cell junction, synapse. Membrane. Nucleus. Cytoplasm. Nuclear localization is induced by TGF-beta.




PMID: 15123989 by Mukhopadhyay A., et al. Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disorders.
PMID: 21228389 by Sultana A., et al. Olfactomedin 2: expression in the eye and interaction with other olfactomedin domain-containing proteins.