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PTHLH

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For Research Use Only. Not For Clinical Use.


Background

The protein encoded by this gene is a member of the parathyroid hormone family. This hormone, via its receptor, PTHR1, regulates endochondral bone development and epithelial-mesenchymal interactions during the formation of the mammary glands and teeth. It is responsible for most cases of humoral hypercalcemia of malignancy, and mutations in this gene are associated with brachydactyly type E2 (BDE2). Alternatively spliced transcript variants have been found for this gene. There is also evidence for alternative translation initiation from non-AUG (CUG and GUG) start sites, downstream of the initiator AUG codon, resulting in nuclear forms of this hormone.
PTHLH
Protein class

Cancer-related genes, Disease related genes, Human disease related genes

Predicted location

Secreted

Single cell type specificity

Cell type enhanced (Basal respiratory cells, Breast glandular cells, Basal squamous epithelial cells, Club cells, Breast myoepithelial cells)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Group enriched (HaCaT, HBEC3-KT)

Interaction

PTHrP interacts with PTH1R (via N-terminal extracellular domain).

Molecular function

Hormone

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