FA58A Polyclonal Antibody, 20ul Supplements HCFC1 is a member of

HCFC1 is a member of the host cell factor family and encodes a protein with five Kelch repeats

Alternate splicing of this gene results in at least two isoforms that localize to the centrosome and the Golgi apparatus

Methyl-CpG-binding domain protein 3 is a subunit of the NuRD

This gene encodes the rate-limiting enzyme of the polyamine biosynthesis pathway which catalyzes ornithine to putrescine

is a lysosomal cysteine proteinase that may play an important role in corneal physiology

FA58A Polyclonal Antibody, 20ul Supplements HCFC1 is a member ofMutations 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.