KALIG-1 Polyclonal Antibody, 20ul Peptide Modification GPR176is a Protein Coding gene

GPR176is a Protein Coding gene

An important paralog of this gene is KHSRP

thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors

Mutations in KRT10 are associated with epidermolytic hyperkeratosis

The encoded protein responds to diverse cellular stresses to regulate expression of target genes

KALIG-1 Polyclonal Antibody, 20ul Peptide Modification GPR176is a Protein Coding geneMutations in KAL1 cause the X linked Kallmann syndrome. Anosmin 1 is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N glycosylated and may have anti protease activity.