Answer:
a. WNT4 protein is encoded by the WNT4 gene it is located in the chromosomes. WNT4 is responsible for the development of female features, while inhibiting the male development. Mutation of WNT4 gene will result in the Rokitansky-Kuster-Hauser syndrome.
b. Located in the 9th chromosome, DMRT1 (Doublesex and mad-3 related transcription factor 1) is the protein encoded by DMRT1 gene, it is responsible for the regulation of the gonadal sex distinction, thus sex (male) determination in multicellular eukaryotes. Mutation of this gene results in the deletion of 9p chromosome, causing abnormal testicular formation since the DMRT1 protein is found in the testicular cord and seritoli cells.
c. FGF9 promotes male sex development. Mutation causes an XY sex reversal.
Step-by-step explanation: