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FAM111B


Official Full Name
FAM111 trypsin like peptidase B
Organism
Homo sapiens
Gene ID
374393
Background
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 trypsinlike peptidase domain, FAM111A, is located only 16 kb from this gene on human chromosome 11q12.1. [provided by RefSeq, Apr 2014]
Synonyms
CANP; POIKTMP

Cat.No. Product Name Price
SHH289133 shRNA set against Human FAM111B (NM_198947.3) Inquiry
Cat.No. Product Name Price
CDFH006318 Human FAM111B cDNA Clone(NM_001142703.1) Inquiry
CDFH006319 Human FAM111B cDNA Clone(NM_001142704.1) Inquiry
MiUTR3H-14799 FAM111B miRNA 3'UTR clone Inquiry
MiUTR3H-14800 FAM111B miRNA 3'UTR clone Inquiry
MiUTR3H-14801 FAM111B miRNA 3'UTR clone Inquiry
CDCR062406 Human FAM111B ORF clone (NM_001142703.1) Inquiry
CDCR351637 Human FAM111B ORF Clone(NM_001142704.1) Inquiry
CDCS408319 Human FAM111B ORF Clone (BC130513) Inquiry
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