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Kallmann Syndrome 1
The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3. (NCI Thesaurus)
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An X-linked or autosomal dominant genetic syndrome characterized by hypogonadotropic hypogonadism and anosmia.
Kallikrein-2 (261 aa, ~29 kDa) is encoded by the human KLK2 gene. This protein plays a role in proteolysis and vasodilation. …
Kallikrein-15 (256 aa, ~28 kDa) is encoded by the human KLK15 gene. This protein is involved in proteolysis.
Kallikrein-11 (282 aa, ~31 kDa) is encoded by the human KLK11 gene. This protein plays a role in peptide metabolism.
Kallikrein-10 (276 aa, ~30 kDa) is encoded by the human KLK10 gene. This protein plays a role in both the mediation of…
One Kallikrein Inhibitor Unit is identical to the quantity of protease inhibitor (eg, aprotinin) that has the ability to inhibit two kallikrein…
