about
Collagen, type II, alpha 1Bone morphogenetic protein 4SMAD family member 1SMAD family member 5SMAD family member 5SMAD family member 9Tumor necrosis factor (ligand) superfamily, member 11Secreted acidic cysteine rich glycoproteinTwist basic helix-loop-helix transcription factor 1Fibroblast growth factor receptor 2Phosphate regulating endopeptidase homolog, X-linkedSteroid 5 alpha-reductase 2Nuclear receptor binding SET domain protein 2Peptidylprolyl isomerase BGuanine nucleotide-binding protein G(s) subunit alpha isoforms XLasTUB like protein 3Natriuretic peptide receptor 2Ankyrin repeat domain 11BBX high mobility group box domain containingMitoguardin 2Guanine nucleotide-binding protein G(s) subunit alpha isoforms shortHomeobox A11Matrix metallopeptidase 14LDL receptor related protein 5Protein ALEXA-kinase anchoring protein 13ASXL transcriptional regulator 1Phosphoribosyl pyrophosphate synthetase associated protein 2Matrix metallopeptidase 16Intraflagellar transport 172Prostaglandin E receptor 4Prolyl 3-hydroxylase 1Thyroid hormone receptor interactor 11Platelet derived growth factor CTetratricopeptide repeat domain 93'-phosphoadenosine 5'-phosphosulfate synthase 2Wnt family member 1Steroid 5 alpha-reductase 1Tripartite motif containing 45Plastin 3
P682
Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar SyndromeStanniocalcin 1 acts as a paracrine regulator of growth plate chondrogenesisDecreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and miceMutations in WNT1 cause different forms of bone fragilityPLS3 mutations in X-linked osteoporosis with fracturesDymeclin, the gene underlying Dyggve-Melchior-Clausen syndrome, encodes a protein integral to extracellular matrix and golgi organization and is associated with protein secretion pathways critical in bone developmentThe effect of Kashin-Beck disease-affected feed and T-2 toxin on the bone development of Wistar rats.SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defectsRPL13 Variants Cause Spondyloepimetaphyseal Dysplasia with Severe Short Stature
P921
Q14877688-6ED0B25D-C888-4F70-890C-FE675C28EB2DQ14903410-CB5FEA9B-4D22-4A24-A8BB-A6C2655AB057Q14903821-EFC02CB5-2725-4AB0-80B5-949F0354C0BCQ14904349-E2997A5A-8430-4DB6-BA0B-3ACF1819D38DQ14904355-39B013D5-33AC-41A5-8412-566A3014A244Q14904387-8502E2CF-6875-49F8-9E17-DDAA8F865B83Q14905570-F5357883-916F-4CFF-9B7A-97D3D07D499AQ14906164-579234C9-9D6A-4331-9C52-0AD9705A6F68Q14906441-2254019A-E790-4DDD-91E8-902FFD8BCBDBQ14911646-7414FA5B-6151-4A80-80ED-9AB7028BF0ACQ14913443-DF7950E4-17AB-4850-B564-603582B98CAEQ15321552-3F7BDD5D-F2B2-48F1-8DF4-4CB38BFFA520Q21097198-85533CCB-A6EB-4006-9615-3107552E6853Q21100333-098EEC30-7517-4478-B45A-1EE3C1C48231Q21102044-BC69516D-575A-440B-B325-05BE6A3D3CB8Q21105140-F6E2E676-A10D-449B-A007-3A12005BFEE5Q21105148-560863B3-5D44-4E65-910C-94F2BFDDA3DBQ21105184-5488C005-E4B9-4D48-8E44-AC833F8EAA14Q21105428-2CD53FF9-3462-4B47-8B45-37E02B8C9545Q21105966-24A4F492-5E8C-4D51-A6A2-54DB46AC1343Q21106183-D52FDCAB-0C95-4B65-85E1-D003A50344A6Q21108742-02D48E36-D896-43B1-913A-4950DAD14018Q21109573-1CC9B67C-C4E2-4D43-89F7-7E04B16CF5E7Q21111886-8B766C28-5737-477D-8DCF-5F7690C7C1C3Q21112590-3E10B4F2-084B-41CE-839D-43FFE98E012EQ21116509-C69B13E8-D1BE-47CC-9DBA-CDBCC375569DQ21116525-AFA0A32F-FBFF-4D77-AF30-682D1FD51A62Q21119237-58104871-1082-4D00-ADF1-C2614EF8B232Q21119466-FE959208-6E6B-4298-8BFC-9A567DE2200DQ21119802-13BEA60C-305B-4242-903F-036F2093C737Q21120422-16742E79-6C1A-490E-87D1-A3CBA540FAD6Q21121809-327FD4F0-2BDC-47B9-B311-5DEBEB14903AQ21122231-4997B587-65D6-419A-A9C9-72A294C8D778Q21123252-C83F8A79-5FE3-4D91-BB39-CA138C66206EQ21123514-0662483B-2A19-4DCE-B564-136ABB3C0368Q21123697-34D755F0-6EBA-42C1-BE0A-5477F0B8B0FBQ21123961-C8852A2F-CC38-4308-B89E-85697045BF5BQ21124444-D7E8D644-D3B2-4EE0-955D-8E6A94820D56Q21124682-D5519BE3-F2FF-41ED-A7DD-57C5245F9E15Q21124930-E4CEDE96-B3B4-4F21-91A7-0DE1181A1E56
P682
description
biologisch proces
@nl
process whose specific outcome ...... mation to the mature structure
@en
name
bone development
@en
desarrollo óseo
@es
développement osseux
@fr
utvikling av knokkel
@nn
развитие костей
@ru
type
label
bone development
@en
desarrollo óseo
@es
développement osseux
@fr
utvikling av knokkel
@nn
развитие костей
@ru
altLabel
GO:0060348
@en
GO:0060348
@nn
beinutvikling
@nn
développement de l'os
@fr
développement des os
@fr
knokkelutvikling
@nn
utvikling av bein
@nn
prefLabel
bone development
@en
desarrollo óseo
@es
développement osseux
@fr
utvikling av knokkel
@nn
развитие костей
@ru
P486
P2888
P486
P686
GO:0060348