Amhr2

Predicted to enable several functions, including anti-Mullerian hormone receptor activity; protein homodimerization activity; and transforming growth factor beta receptor activity, type II. Acts upstream of or within sex differentiation. Predicted to be part of receptor complex. Predicted to be active in plasma membrane. Is expressed in several structures, including bone; early embryo; forebrain; genitourinary system; and spinal cord lumbar region. Used to study persistent Mullerian duct syndrome. Human ortholog(s) of this gene implicated in persistent Mullerian duct syndrome. Orthologous to human AMHR2 (anti-Mullerian hormone receptor type 2). [provided by Alliance of Genome Resources, Nov 2024]

预计该基因能激活多种功能，包括抗缪勒氏管激素受体活性、蛋白质同源二聚化活性以及转化生长因子β受体活性（II型）。该基因在性别分化的上游或其中发挥作用。预计该基因参与受体复合体的组成。预计在质膜上具有活性。在多个结构中表达，包括骨骼、早期胚胎、前脑、泌尿生殖系统和脊髓腰段。用于研究持续性缪勒氏管综合征。该基因的人类同源基因与持续性缪勒氏管综合征相关。与人类AMHR2（抗缪勒氏管激素受体2型）同源。[由基因组资源联盟提供，2024年11月]