Type | Description |
---|---|
Definition | formiminotransferase cyclodeaminase N-terminal like |
Date | Results | Publications |
---|---|---|
2016-06-28 11:44:00 | rs10203122 in FTCDNL1 is associated with a susceptibility to osteoporosis. | 26492493 |
2013-07-27 12:23:00 | results suggest that Japanese subjects homozygous for the risk alleles of rs7605378 in FONG and rs12673629 in THSD7A have a significantly higher risk of vertebral fracture | 23303384 |
2011-09-03 11:39:00 | A single nucleotide polymorphism (SNP), rs7605378 associated with osteoporosis, was identified, in a previously unknown gene on chromosome 2q33.1, FONG. | 21573128 |
Type | IDs |
---|---|
Synonymous | FONG |
Gene | |
Nucleutide sequences | |
Protein sequencees |
RefSeq:
XP_024308623.1,
XP_024308628.1,
XP_024308621.1,
XP_024308638.1,
XP_024308625.1,
XP_024308637.1,
NP_001337783.1,
XP_024308640.1,
NP_001350815.1,
XP_024308636.1,
XP_024308627.1,
XP_024308633.1,
XP_024308639.1,
XP_024308632.1,
NP_001337784.1,
XP_024308635.1,
XP_024308629.1,
XP_024308641.1,
NP_001337782.1,
XP_024308631.1,
XP_024308626.1,
XP_024308620.1,
XP_024308622.1,
XP_024308634.1
|
Others |
UniGene:
Hs.734578
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
{{protein.nucleotideVersion}}
Ensembl: {{protein.nucleotideEnsembl}} |
{{protein.proteinVersion}}
Ensembl: {{protein.proteinEnsembl}} |
{{uniprot}} , |
Definition: {{{protein.definition}}}Transcript Veriant:{{protein.transcriptVeriant}} Status: {{protein.status}} |
||||
Location | {{protein.contigId}} ( {{protein.positionStart}}..{{protein.positionEnd}} , {{protein.orientation}} ) | |||||||
Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
{{conservedDomain.comments == '' || conservedDomain.comments == null ? "-" : conservedDomain.comments }} |
Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
{{conservedDomain.comments == '' || conservedDomain.comments == null ? "-" : conservedDomain.comments }} |
暂无数据
Pubmed编号 | 文献信息 | 发表日期 | 相关基因 |
---|---|---|---|
26492493 |
Association Study between the FTCDNL1 (FONG) and Susceptibility to Osteoporosis. PLoS One Hsing-Fang Lu , Kuo-Sheng Hung , Yu-Wen Hsu , Yu-Ting Tai , Lin-Shan Huang , Yu-Jia Wang , Henry Sung-Ching Wong , Yi-Hsiang Hsu , Wei-Chiao Chang |
2015-01-01 | - |
23974872 |
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet Stephan Ripke , Colm O'Dushlaine , Kimberly Chambert , Jennifer L Moran , Anna K Kähler , Susanne Akterin , Sarah E Bergen , Ann L Collins , James J Crowley , Menachem Fromer , Yunjung Kim , Sang Hong Lee , Patrik K E Magnusson , Nick Sanchez , Eli A Stahl , Stephanie Williams , Naomi R Wray , Kai Xia , Francesco Bettella , Anders D Borglum , Brendan K Bulik-Sullivan , Paul Cormican , Nick Craddock , Christiaan de Leeuw , Naser Durmishi , Michael Gill , Vera Golimbet , Marian L Hamshere , Peter Holmans , David M Hougaard , Kenneth S Kendler , Kuang Lin , Derek W Morris , Ole Mors , Preben B Mortensen , Benjamin M Neale , Francis A O'Neill , Michael J Owen , Milica Pejovic Milovancevic , Danielle Posthuma , John Powell , Alexander L Richards , Brien P Riley , Douglas Ruderfer , Dan Rujescu , Engilbert Sigurdsson , Teimuraz Silagadze , August B Smit , Hreinn Stefansson , Stacy Steinberg , Jaana Suvisaari , Sarah Tosato , Matthijs Verhage , James T Walters , Multicenter Genetic Studies of Schizophrenia Consortium , Douglas F Levinson , Pablo V Gejman , Kenneth S Kendler , Claudine Laurent , Bryan J Mowry , Michael C O'Donovan , Michael J Owen , Ann E Pulver , Brien P Riley , Sibylle G Schwab , Dieter B Wildenauer , Frank Dudbridge , Peter Holmans , Jianxin Shi , Margot Albus , Madeline Alexander , Dominique Campion , David Cohen , Dimitris Dikeos , Jubao Duan , Peter Eichhammer , Stephanie Godard , Mark Hansen , F Bernard Lerer , Kung-Yee Liang , Wolfgang Maier , Jacques Mallet , Deborah A Nertney , Gerald Nestadt , Nadine Norton , Francis A O'Neill , George N Papadimitriou , Robert Ribble , Alan R Sanders , Jeremy M Silverman , Dermot Walsh , Nigel M Williams , Brandon Wormley , Psychosis Endophenotypes International Consortium , Maria J Arranz , Steven Bakker , Stephan Bender , Elvira Bramon , David Collier , Benedicto Crespo-Facorro , Jeremy Hall , Conrad Iyegbe , Assen Jablensky , Rene S Kahn , Luba Kalaydjieva , Stephen Lawrie , Cathryn M Lewis , Kuang Lin , Don H Linszen , Ignacio Mata , Andrew McIntosh , Robin M Murray , Roel A Ophoff , John Powell , Dan Rujescu , Jim Van Os , Muriel Walshe , Matthias Weisbrod , Durk Wiersma , Wellcome Trust Case Control Consortium 2 , Peter Donnelly , Ines Barroso , Jenefer M Blackwell , Elvira Bramon , Matthew A Brown , Juan P Casas , Aiden P Corvin , Panos Deloukas , Audrey Duncanson , Janusz Jankowski , Hugh S Markus , Christopher G Mathew , Colin N A Palmer , Robert Plomin , Anna Rautanen , Stephen J Sawcer , Richard C Trembath , Ananth C Viswanathan , Nicholas W Wood , Chris C A Spencer , Gavin Band , Céline Bellenguez , Colin Freeman , Garrett Hellenthal , Eleni Giannoulatou , Matti Pirinen , Richard D Pearson , Amy Strange , Zhan Su , Damjan Vukcevic , Peter Donnelly , Cordelia Langford , Sarah E Hunt , Sarah Edkins , Rhian Gwilliam , Hannah Blackburn , Suzannah J Bumpstead , Serge Dronov , Matthew Gillman , Emma Gray , Naomi Hammond , Alagurevathi Jayakumar , Owen T McCann , Jennifer Liddle , Simon C Potter , Radhi Ravindrarajah , Michelle Ricketts , Avazeh Tashakkori-Ghanbaria , Matthew J Waller , Paul Weston , Sara Widaa , Pamela Whittaker , Ines Barroso , Panos Deloukas , Christopher G Mathew , Jenefer M Blackwell , Matthew A Brown , Aiden P Corvin , Mark I McCarthy , Chris C A Spencer , Elvira Bramon , Aiden P Corvin , Michael C O'Donovan , Kari Stefansson , Edward Scolnick , Shaun Purcell , Steven A McCarroll , Pamela Sklar , Christina M Hultman , Patrick F Sullivan |
2013-10-01 | - |
23648065 |
Cancer Sci. Siew-Kee Low , Suyoun Chung , Atsushi Takahashi , Hitoshi Zembutsu , Taisei Mushiroda , Michiaki Kubo , Yusuke Nakamura |
2013-08-01 |
LOC100129345,
LOC100129620,
SNAP25-AS1,
LOC100131425,
LOC100131680,
GNG12-AS1,
MIR2113,
LOC100420587,
LOC100421527,
LOC100505995,
LOC100506098,
LOC101928667,
LOC101929200,
LOC101929241,
LOC102723507,
VAV3,
AGR2,
ME3,
PRSS23,
ATP6V1G3,
CHODL,
LOC151121,
DAB2IP,
ADAMTS18,
SRSF10P2,
EBF1,
ESRRG,
GSX1,
GPC5,
MLXIP,
FOXI1,
FLNB,
KIAA0922,
KAZN,
LRRC8B,
OSBP2,
FSHR,
ALPL,
AKNAD1,
GALC,
ULK3,
LRIG1,
FAM50B,
SIT1,
PRTG,
LOC284294,
SCARA5,
GRM7,
HOXC13,
MACC1,
FTCDNL1,
RPS16P2,
MATN2,
RPL36AP45,
CRYL1,
PDE4D,
HMP19,
SERPINE2,
PLCG2,
TMEM106B,
FGD6,
ERGIC1,
ALPK3,
RXRA,
PRDM1,
LHPP,
CSMD1,
RPL13AP3,
LOC651644,
SLC13A1,
TRA,
TNFRSF1A,
ZNF236,
SPEF2,
DENND1C,
WLS,
CMIP,
APOL3,
PTPN5,
GAS7,
RAB9BP1,
ARHGAP18,
NCOR2,
ZNF536,
ARHGAP44,
HS3ST2
|
23303384 |
J Hum Genet Heying Zhou , Seijiro Mori , Ikuyo Kou , Noriyuki Fuku , Makiko Naka Mieno , Naoko Honma , Tomio Arai , Motoji Sawabe , Masashi Tanaka , Shiro Ikegawa , Hideki Ito |
2013-02-01 | - |
21573128 |
Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese. PLoS One Ikuyo Kou , Atsushi Takahashi , Tomohiko Urano , Naoshi Fukui , Hideki Ito , Kouichi Ozaki , Toshihiro Tanaka , Takayuki Hosoi , Masataka Shiraki , Satoshi Inoue , Yusuke Nakamura , Naoyuki Kamatani , Michiaki Kubo , Seijiro Mori , Shiro Ikegawa |
2011-05-06 | - |
12477932 |
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc. Natl. Acad. Sci. U.S.A. Robert L Strausberg , Elise A Feingold , Lynette H Grouse , Jeffery G Derge , Richard D Klausner , Francis S Collins , Lukas Wagner , Carolyn M Shenmen , Gregory D Schuler , Stephen F Altschul , Barry Zeeberg , Kenneth H Buetow , Carl F Schaefer , Narayan K Bhat , Ralph F Hopkins , Heather Jordan , Troy Moore , Steve I Max , Jun Wang , Florence Hsieh , Luda Diatchenko , Kate Marusina , Andrew A Farmer , Gerald M Rubin , Ling Hong , Mark Stapleton , M Bento Soares , Maria F Bonaldo , Tom L Casavant , Todd E Scheetz , Michael J Brownstein , Ted B Usdin , Shiraki Toshiyuki , Piero Carninci , Christa Prange , Sam S Raha , Naomi A Loquellano , Garrick J Peters , Rick D Abramson , Sara J Mullahy , Stephanie A Bosak , Paul J McEwan , Kevin J McKernan , Joel A Malek , Preethi H Gunaratne , Stephen Richards , Kim C Worley , Sarah Hale , Angela M Garcia , Laura J Gay , Stephen W Hulyk , Debbie K Villalon , Donna M Muzny , Erica J Sodergren , Xiuhua Lu , Richard A Gibbs , Jessica Fahey , Erin Helton , Mark Ketteman , Anuradha Madan , Stephanie Rodrigues , Amy Sanchez , Michelle Whiting , Anup Madan , Alice C Young , Yuriy Shevchenko , Gerard G Bouffard , Robert W Blakesley , Jeffrey W Touchman , Eric D Green , Mark C Dickson , Alex C Rodriguez , Jane Grimwood , Jeremy Schmutz , Richard M Myers , Yaron S N Butterfield , Martin I Krzywinski , Ursula Skalska , Duane E Smailus , Angelique Schnerch , Jacqueline E Schein , Steven J M Jones , Marco A Marra , Mammalian Gene Collection Program Team |
2002-12-24 | - |
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