ABHD4 Polyclonal Antibody, 100ul Antibody Humanization Mutations in this gene cause

Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness

This gene belongs to the non-CT (non cancer/testis) subgroup of the melanoma-associated antigen (MAGE) superfamily

FOXN2 encodes a forkhead domain binding protein and may function in the transcriptional regulation of the human T-cell leukemia virus long terminal repeat

and mutations in this gene have been associated with different neuromuscular diseases

but binds only retinoic acid at specific sites within the nucleus

ABHD4 Polyclonal Antibody, 100ul Antibody Humanization Mutations in this gene causeABHD4 (Abhydrolase Domain Containing 4) is a Protein Coding gene. Among its related pathways are Glycerophospholipid biosynthesis and Metabolism. GO annotations related to this gene include hydrolase activity and 1 alkyl 2 acetylglycerophosphocholine esterase activity. An important paralog of this gene is ABHD5.