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FAM58A


Official Full Name
cyclin Q
Organism
Homo sapiens
Gene ID
92002
Background
Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
Synonyms
CCNQ; CycM; FAM58A

Cat.No. Product Name Price
SHH291385 shRNA set against Human FAM58A (NM_152274.3) Inquiry
SHW008684 shRNA set against Danio rerio FAM58A (NM_001020623) Inquiry
Cat.No. Product Name Price
CDCB170159 Danio rerio FAM58A ORF Clone (NM_001020623) Inquiry
CDFG009321 Human FAM58A cDNA Clone(NM_152274.3) Inquiry
CDFH006519 Human FAM58A cDNA Clone(NM_001130997.1) Inquiry
MiUTR3H-02915 FAM58A miRNA 3'UTR clone Inquiry
MiUTR3H-02916 FAM58A miRNA 3'UTR clone Inquiry
CDCB186061 Rabbit FAM58A ORF clone (XM_002722631.2) Inquiry
CDCR063362 Human FAM58A ORF clone (NM_152274.3) Inquiry
CDCR063364 Human FAM58A ORF clone (NM_001130997.1) Inquiry
CDCS418576 Human FAM58A ORF Clone (BC001909) Inquiry
CDCS418577 Human FAM58A ORF Clone (BC007232) Inquiry
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