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

Defects in this gene are implicated in a variety of cancers

Mutations in SLC5A1 have been associated with glucose-galactose malabsorption

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

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

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

FAM3D Polyclonal Antibody, 50ul[BT-AP03151] RNA Synthesis Defects in this gene areFAM3D (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.