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Rabbit Anti-KIAA1191 antibody
KIAA1199 belongs to the TMEM2 family and contains 4 PbH1 repeats. It is expressed in the inner ear. It is expressed in cochlea and vestibule tissues and it may be involved in hearing. Defects in KIAA1199 may be a cause of non-syndromic hearing loss. It is also thought that KIAA1199 is a tumor suppressor that may be involved in establishing cellular mortality in normal human cells.
Function:
Potential NADPH-dependent oxidoreductase. May be involved in the regulation of neuronal survival, differentiation and axonal outgrowth.
Subunit:
Interacts with COBRA1, NOL12 and PRNP.
Tissue Specificity:
Down-regulated in the occipital lobe of an early stage Alzheimer disease patients.
Similarity:
Belongs to the P33MONOX family.
SWISS:
Q96A73
Gene ID:
57179
Database links:
Entrez Gene: 57179 Human
SwissProt: Q96A73 Human
Unigene: 519783 Human
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