This gene encodes a secreted member of the insulin growth factor-binding protein (IGFBP) superfamily. The protein contains an insulin growth factor-binding domain in its N-terminal region, a Kazal-type serine protease inhibitor and follistatin-like domain in its central region, and an immunoglobulin-like domain in its C-terminal region. Studies of the mouse ortholog suggest that this protein may function in bone development and bone regeneration. This gene is hypomethylated and over-expressed in high-grade glioma compared to low-grade glioma, and thus the hypomethylated gene may be associated with cell proliferation and the shorter survival of patients with high-grade glioma. It is also one of numerous genes found to be deleted in a novel 5.54 Mb interstitial deletion, which is associated with multiple congenital anomalies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
KAZALD1-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
KAZALD1-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
KAZALD1-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
KAZALD1-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
KAZALD1-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a secreted member of the insulin growth factor-binding protein (IGFBP) superfamily. The protein contains an insulin growth factor-binding domain in its N-terminal region, a Kazal-type serine protease inhibitor and follistatin-like domain in its central region, and an immunoglobulin-like domain in its C-terminal region. Studies of the mouse ortholog suggest that this protein may function in bone development and bone regeneration. This gene is hypomethylated and over-expressed in high-grade glioma compared to low-grade glioma, and thus the hypomethylated gene may be associated with cell proliferation and the shorter survival of patients with high-grade glioma. It is also one of numerous genes found to be deleted in a novel 5.54 Mb interstitial deletion, which is associated with multiple congenital anomalies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Gene Symbol : KAZALD1
Gene Name : Kazal type serine peptidase inhibitor domain 1
Chromosome : CHR 10: 101,061,140-101,068,140
Locus : 10q24.31
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