<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao F</submitter><funding>NICHD NIH HHS</funding><pagination>23037</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4786858</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6</volume><pubmed_abstract>Congenital reproductive tract anomalies could impair fertility. Female and male reproductive tracts are developed from Müllerian ducts and Wolffian ducts, respectively, involving initiation, elongation and differentiation. Genetic basis solely for distal reproductive tract development is largely unknown. Lhfpl2 (lipoma HMGIC fusion partner-like 2) encodes a tetra-transmembrane protein with unknown functions. It is expressed in follicle cells of ovary and epithelial cells of reproductive tracts. A spontaneous point mutation of Lhfpl2 (LHFPL2(G102E)) leads to infertility in 100% female mice, which have normal ovarian development, ovulation, uterine development, and uterine response to exogenous estrogen stimulation, but abnormal upper longitudinal vaginal septum and lower vaginal agenesis. I</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Novel function of LHFPL2 in female and male distal reproductive tract development.</pubmed_title><pmcid>PMC4786858</pmcid><funding_grant_id>R01 HD065939</funding_grant_id><funding_grant_id>R15HD066301</funding_grant_id><funding_grant_id>R01HD065939</funding_grant_id><funding_grant_id>R15 HD066301</funding_grant_id><pubmed_authors>Dudley EA</pubmed_authors><pubmed_authors>Zhao F</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Ye X</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Novel function of LHFPL2 in female and male distal reproductive tract development.</name><description>Congenital reproductive tract anomalies could impair fertility. Female and male reproductive tracts are developed from Müllerian ducts and Wolffian ducts, respectively, involving initiation, elongation and differentiation. Genetic basis solely for distal reproductive tract development is largely unknown. Lhfpl2 (lipoma HMGIC fusion partner-like 2) encodes a tetra-transmembrane protein with unknown functions. It is expressed in follicle cells of ovary and epithelial cells of reproductive tracts. A spontaneous point mutation of Lhfpl2 (LHFPL2(G102E)) leads to infertility in 100% female mice, which have normal ovarian development, ovulation, uterine development, and uterine response to exogenous estrogen stimulation, but abnormal upper longitudinal vaginal septum and lower vaginal agenesis. I</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2025-04-18T22:04:19.653Z</modification><creation>2019-03-27T02:10:52Z</creation></dates><accession>S-EPMC4786858</accession><cross_references><pubmed>26964900</pubmed><doi>10.1038/srep23037</doi></cross_references></HashMap>