호모 사피엔스 종의 유전자
Bardet-Biedl 증후군 9는 BBS9 [4] [5] 유전자에 의해 인간에게 암호화되는 단백질 이다.
Bardet-Biedl 증후군 9 단백질의 발현은 골아세포 의 부갑상선 호르몬 에 의해 하향 조절되므로 [6] 뼈의 부갑상선 호르몬 작용에 관여하는 것으로 생각된다.
이 유전자의 돌연변이는 바르데-비들 [5] 증후군과 관련이 있다.
레퍼런스 ^ a b c GRCm38: 앙상블 릴리즈 89: ENSMUSG000035919 - 앙상블 , 2017년 5월 ^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine . ^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine . ^ Adams AE, Rosenblatt M, Suva LJ (April 1999). "Identification of a novel parathyroid hormone-responsive gene in human osteoblastic cells". Bone . 24 (4): 305–13. doi :10.1016/S8756-3282(98)00188-4 . PMID 10221542 . ^ a b Nishimura DY, Swiderski RE, Searby CC, Berg EM, Ferguson AL, Hennekam R, Merin S, Weleber RG, Biesecker LG, Stone EM, Sheffield VC (December 2005). "Comparative genomics and gene expression analysis identifies BBS9, a new Bardet–Biedl syndrome gene" . Am. J. Hum. Genet . 77 (6): 1021–33. doi :10.1086/498323 . PMC 1285160 . PMID 16380913 . ^ "Entrez Gene: Bardet–Biedl syndrome 9" . 외부 링크
추가 정보 Scherer SW, Cheung J, MacDonald JR, et al. (2003). "Human chromosome 7: DNA sequence and biology" . Science . 300 (5620): 767–72. Bibcode :2003Sci...300..767S . doi :10.1126/science.1083423 . PMC 2882961 . PMID 12690205 . Kang H, Lee SK, Kim MH, et al. (2008). "Parathyroid hormone-responsive B1 gene is associated with premature ovarian failure" . Hum. Reprod . 23 (6): 1457–65. doi :10.1093/humrep/den086 . PMID 18349106 . Nachury MV, Loktev AV, Zhang Q, et al. (2007). "A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis" . Cell . 129 (6): 1201–13. doi :10.1016/j.cell.2007.03.053 . PMID 17574030 . S2CID 11917072 . Vernon EG, Malik K, Reynolds P, et al. (2003). "The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour" . Oncogene . 22 (9): 1371–80. doi :10.1038/sj.onc.1206332 . PMID 12618763 . Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)" . Genome Res . 14 (10B): 2121–7. doi :10.1101/gr.2596504 . PMC 528928 . PMID 15489334 . Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs" . Nat. Genet . 36 (1): 40–5. doi :10.1038/ng1285 . PMID 14702039 . Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences" . Proc. Natl. Acad. Sci. U.S.A . 99 (26): 16899–903. Bibcode :2002PNAS...9916899M . doi :10.1073/pnas.242603899 . PMC 139241 . PMID 12477932 . 외부 링크