Tissue expression
Cell line expression
Protein structure
FAM111B
Family with sequence similarity 111 member BCANP
This gene encodes a protein with a trypsin-like cysteine/serine peptidase domain in the C-terminus. Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP). Affected individuals display mottled pigmentation, telangiectasia, epidermal atrophy, tendon contractures, and progressive pulmonary fibrosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A paralog of this gene which also has a trypsin‐like peptidase domain, FAM111A, is located only 16 kb from this gene on human chromosome 11q12.1. [provided by RefSeq, Apr 2014]
Top validated antibodies |
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Invitrogen Antibodies | PA5-58474 | 1 references | Polyclonal |
WB
ICC
IHC
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NovoPro Bioscience Inc. | 110459 | Polyclonal |
WB
EL
ICC
IHC |
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antibodies-online | ABIN787163 | Monoclonal |
WB
ICC
IHC
|
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FineTest Biotech | FNab02954 | Polyclonal |
WB
EL
ICC
IHC |
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GeneTex | GTX107084 | Polyclonal |
WB
ICC
IHC
|
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