KCTD13 (NP_849194, 24 a.a. ~ 119 a.a) partial recombinant protein with GST tag. The sequence is LEPGPAAYGLKPLTPNSKYVKLNVGGSLHYTTLRTLTGQDTMLKAMFSGRVEVLTDAGGW VLIDRSGRHFGTILNYLRDGSVPLPESTRELGELLG
Conjugate
Unconjugated
Target
Alternative Names
KCTD13; potassium channel tetramerization domain containing 13; PDIP1; FKSG86; BACURD1; POLDIP1; hBACURD1; BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 1; TNFAIP1-like protein; polymerase delta-interacting protein 1; BTB/PO
KCTD13 (potassium channel tetramerization domain containing 13) is a protein-coding gene. Diseases associated with KCTD13 include microcephaly, and maturity-onset diabetes of the young, and among its related super-pathways are Melatonin Signaling and Activation of cAMP-Dependent PKA. GO annotations related to this gene include identical protein binding and protein domain specific binding. An important paralog of this gene is TNFAIP1.
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