A novel human gene FKBP6 is deleted in Williams syndrome.Meng X., Lu X., Morris C.A., Keating M.T.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)TissueTestisCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenomics 52:130-137 (1998)Cited in1
No title available.Zan Q., Guo J.H., Yu L.Cited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Submission Submitted to EMBL/GenBank/DDBJ databases (NOV-2001)Cited in92
Complete sequencing and characterization of 21,243 full-length human cDNAs.Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H.[...], Sugano S.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2)TissueTestisCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Genet. 36:40-45 (2004)Cited in99+99+
The DNA sequence of human chromosome 7.Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S.[...], Wilson R.K.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 424:157-164 (2003)Cited in99+99+
No title available.Mural R.J., Istrail S., Sutton G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H.[...], Venter J.C.Cited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Submission Submitted to EMBL/GenBank/DDBJ databases (SEP-2005)Cited in99+99+
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).The MGC Project TeamView abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1)TissueBrainCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
Autosomal dominant inheritance of Williams-Beuren syndrome in a father and son with haploinsufficiency for FKBP6.Metcalfe K., Simeonov E., Beckett W., Donnai D., Tassabehji M.View abstractCited forPOSSIBLE INVOLVEMENT IN WBSCategoriesDisease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCClin. Dysmorphol. 14:61-65 (2005)Cited in1
Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia.Westerveld G.H., Repping S., Lombardi M.P., van der Veen F.View abstractCited forVARIANT CYS-183CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCMol. Hum. Reprod. 11:673-675 (2005)Cited in1
Mutation screening of the FKBP6 gene and its association study with spermatogenic impairment in idiopathic infertile men.Zhang W., Zhang S., Xiao C., Yang Y., Zhoucun A.View abstractCited forINVOLVEMENT IN SPGF77CategoriesDisease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCReproduction 133:511-516 (2007)Cited in1
FKBP36 forms complexes with clathrin and Hsp72 in spermatocytes.Jarczowski F., Fischer G., Edlich F.View abstractCited forINTERACTION WITH HSPA2 AND CLTCCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiochemistry 47:6946-6952 (2008)Cited in3Mapped to6
FKBP36 is an inherent multifunctional glyceraldehyde-3-phosphate dehydrogenase inhibitor.Jarczowski F., Jahreis G., Erdmann F., Schierhorn A., Fischer G., Edlich F.View abstractCited forINTERACTION WITH GAPDHCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 284:766-773 (2009)Cited in2
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans.Genetics of Male Infertility Initiative (GEMINI) consortiumWyrwoll M.J., Gaasbeek C.M., Golubickaite I., Stakaitis R., Oud M.S., Nagirnaja L., Dion C., Sindi E.B., Leitch H.G.[...], van der Heijden G.W.View abstractCited forVARIANTS SPGF77 204-ARG--SER-327 DEL AND 278-ARG--SER-327 DEL, INVOLVEMENT IN SPGF77, FUNCTION, SUBCELLULAR LOCATIONCategoriesFunction, Sequences, Disease & Variants, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCAm. J. Hum. Genet. 109:1850-1866 (2022)Cited in1