FAM3D Polyclonal Antibody, 50ul[BT-AP03151] RNA Synthesis Mutations in this gene result

Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy

Reduced levels of mRNA expressed by this gene were found in HD patients

and expressed in testis and in a significant fraction of tumors of various histological types

Mutations in SLC5A1 have been associated with glucose-galactose malabsorption

which includes tumor necrosis factor receptor 1 (TNFR1A) and RIPK1/RIP kinase

FAM3D Polyclonal Antibody, 50ul[BT-AP03151] RNA Synthesis Mutations in this gene resultFAM3D (Family With Sequence Similarity 3 Member D) is a Protein Coding gene. Diseases associated with FAM3D include narcolepsy. GO annotations related to this gene include cytokine activity. An important paralog of this gene is FAM3B.