Why is "Anosmin-1" trending?
Latest news, Wikipedia summary, and trend analysis.
Trend Analysis
- Ranking position: #
- Date: 2026-06-24 10:38:14
This topic has appeared in the trending rankings 1 time(s) in the past year. While it does not trend frequently, its appearance suggests a renewed or concentrated surge of public interest.
Based on Wikipedia pageviews and search interest, this topic gained significant attention on the selected date.
Trend Insight
Anosmin-1 entered the ranking for the first time today at position #. This is its highest position ever recorded.
Trend History
This topic has appeared in the English Wikipedia rankings 1 time. It first appeared on 2026-06-24 and was most recently seen on 2026-06-24.
Wikipedia Overview
Anosmin-1 is a secreted, EM associated glycoprotein found in humans and other organisms responsible for normal development, which is expressed in the brain, spinal cord and kidney. Absence or damage to the protein results in Kallmann syndrome in humans, which is characterized by loss of olfactory bulbs and GnRH secretion leading to anosmia and hypothalamic hypogonadotropic hypogonadism. Anosmin-1 is coded by the ANOS1 gene, which is found on the X chromosome. Anosmin-1 is 100 kilodaltons and is expressed on the outside of cells. Because of this and because of its contribution to normal migration of nerve cells, a role in the extracellular matrix has been postulated.
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Trending Topic Today
Search Interest Perspective
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RoboA reinforces planarian stem cell fate through FoxA and Anosmin1a - Nature
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Anosmin-1 activates vascular endothelial growth factor receptor and its related signaling pathway for olfactory bulb angiogenesis - Nature
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Neurite Branching Regulated by Neuronal Cell Surface Molecules in Caenorhabditis elegans - Frontiers
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Ear and kidney syndromes: Molecular versus clinical approach - ScienceDirect.com
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Four reasons why some people become ‘super smellers’ – from pregnancy to genetic differences - The Conversation
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The effect of glia-glia interactions on oligodendrocyte precursor cell biology during development and in demyelinating diseases - Frontiers
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Point mutations in KAL1 and the mitochondrial gene MT-tRNA - Nature
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A novel KAL1 mutation is associated with combined pituitary hormone deficiency - Nature
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Axonal branching in lateral olfactory tract is promoted by Nogo signaling - Nature
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Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome - Nature
Why This Topic Is Trending
This topic has recently gained attention due to increased public interest. Search activity and Wikipedia pageviews suggest growing global engagement.
Search Interest & Related Topics
Search interest data over the past 12 months indicates that this topic periodically attracts global attention. Sudden spikes often correlate with major news events, public statements, or geopolitical developments.