Details for: BMP15
Associated with
Other Information
Genular Protein ID: 4291180405
Symbol: BMP15_HUMAN
Name: Bone morphogenetic protein 15
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9849956
Title: The bone morphogenetic protein 15 gene is X-linked and expressed in oocytes.
PubMed ID: 9849956
PubMed ID: 10443672
Title: Human growth differentiation factor 9 (GDF-9) and its novel homolog GDF-9B are expressed in oocytes during early folliculogenesis.
PubMed ID: 10443672
PubMed ID: 15772651
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 18227435
Title: Characterization of the post-translational modification of recombinant human BMP-15 mature protein.
PubMed ID: 18227435
DOI: 10.1110/ps.073232608
PubMed ID: 21970812
Title: The ratio of growth differentiation factor 9: bone morphogenetic protein 15 mRNA expression is tightly co-regulated and differs between species over a wide range of ovulation rates.
PubMed ID: 21970812
PubMed ID: 15136966
Title: Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene.
PubMed ID: 15136966
DOI: 10.1086/422103
PubMed ID: 16645022
Title: Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.
PubMed ID: 16645022
DOI: 10.1530/eje.1.02135
PubMed ID: 16508750
Title: Missense mutations in the BMP15 gene are associated with ovarian failure.
PubMed ID: 16508750
PubMed ID: 16464940
Title: Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure.
PubMed ID: 16464940
DOI: 10.1210/jc.2005-2650
PubMed ID: 19263482
Title: BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein.
PubMed ID: 19263482
DOI: 10.1002/humu.20961
PubMed ID: 19438907
Title: Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure.
PubMed ID: 19438907
PubMed ID: 28585349
Title: CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsy.
PubMed ID: 28585349
DOI: 10.1002/humu.23270
Sequence Information:
- Length: 392
- Mass: 45055
- Checksum: A957275EF275A2E8
- Sequence:
MVLLSILRIL FLCELVLFME HRAQMAEGGQ SSIALLAEAP TLPLIEELLE ESPGEQPRKP RLLGHSLRYM LELYRRSADS HGHPRENRTI GATMVRLVKP LTNVARPHRG TWHIQILGFP LRPNRGLYQL VRATVVYRHH LQLTRFNLSC HVEPWVQKNP TNHFPSSEGD SSKPSLMSNA WKEMDITQLV QQRFWNNKGH RILRLRFMCQ QQKDSGGLEL WHGTSSLDIA FLLLYFNDTH KSIRKAKFLP RGMEEFMERE SLLRRTRQAD GISAEVTASS SKHSGPENNQ CSLHPFQISF RQLGWDHWII APPFYTPNYC KGTCLRVLRD GLNSPNHAII QNLINQLVDQ SVPRPSCVPY KYVPISVLMI EANGSILYKE YEGMIAESCT CR
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.