AutismKB 2.0

Annotation Detail for FGF12


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Basic Information Top
Gene Symbol:FGF12 ( FGF12B,FHF1 )
Gene Full Name: fibroblast growth factor 12
Band: 3q28-q29
Quick LinksEntrez ID:2257; OMIM: 601513; Uniprot ID:FGF12_HUMAN; ENSEMBL ID: ENSG00000114279; HGNC ID: 3668
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
38Bipartite nuclear localization signal
Location(AA) Modifications Resource
Location(AA) Modification Resource
32Phosphoserine(PKG)HMM predict
32Phosphoserine(CDC2)HMM predict
101Phosphoserine(CK1)HMM predict
103Phosphotyrosine(INSR)HMM predict
126Phosphotyrosine(INSR)HMM predict
155Phosphotyrosine(Syk)HMM predict
164Phosphotyrosine(Abl)HMM predict
227Phosphoserine(PKB)HMM predict
227Phosphoserine(IKK)HMM predict
227Phosphoserine(PKG)HMM predict
227Phosphoserine(PKC)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_004113
  • Location:chr3 193342423-193928065
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Pol2 GM12878GSE19551 193930013 193930138 125 2010
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 193644965 193645399 434 0
CTCF CD4GSE12889 193667693 193668139 446 0
CTCF CD4GSE12889 193767246 193767516 270 0
CTCF CD4SISSRdata 193644965 193645399 434 0
CTCF CD4SISSRdata 193667693 193668139 446 0
CTCF CD4SISSRdata 193767246 193767516 270 0
CTCF JurkatGSE12889 193644952 193645260 308 0
CTCF G2GSE9613 193608579 193610660 2081 0
CTCF G2GSE9613 193611050 193611286 236 0
CTCF G2GSE9613 193623297 193623500 203 0
CTCF G2GSE9613 193644431 193645330 899 0
CTCF G2GSE9613 193667865 193668320 455 0
CTCF G2GSE9613 193714710 193715006 296 0
CTCF G2GSE9613 193715470 193715900 430 0
CTCF G2GSE9613 193754696 193754974 278 0
CTCF G2GSE9613 193766793 193767652 859 0
CTCF G2GSE9613 193771756 193772149 393 0
CTCF G2GSE9613 193807606 193807850 244 0
CTCF G2GSE9613 193852680 193852825 145 0
CTCF G2GSE9613 193884446 193884842 396 0
CTCF G2GSE9613 193887990 193888816 826 0
FOXA1 MCF7GSE15244 193669993 193670205 212 0
FOXA1 MCF7GSE15244 193797844 193799302 1458 0
FoxA1 MCF7MACSdata 193798025 193798530 505 0
NRSF JurkatGSE13047 193632476 193632737 261 0
NRSF JurkatGSE13047 193714210 193715024 814 0
NRSF JurkatGSE13047 193927751 193928208 457 0
NRSF JurkatSISSRdata 193714378 193715030 652 0
NRSF mAbJurkat 193631921 193632835 914 0
NRSF mAbJurkat 193633395 193633649 254 0
NRSF mAbJurkat 193711461 193712878 1417 0
NRSF mAbJurkat 193713182 193714856 1674 0
NRSF-mono JurkatQuESTdata 193632475 193632736 261 0
NRSF-mono JurkatQuESTdata 193714360 193715017 657 0
NRSF-mono JurkatQuESTdata 193927755 193928237 482 0
NRSF-poly JurkatQuESTdata 193714365 193715303 938 0
NRSF-poly JurkatQuESTdata 193927823 193928107 284 0
Nanog ESGSE20650 193617339 193617876 537 0
Nanog hESGSE18292 193880951 193881372 421 0
Oct4 hESGSE21916 193617461 193617834 373 0
RARA MCF7GSE15244 193797117 193797337 220 0
RARA MCF7GSE15244 193797698 193799302 1604 0
RARG MCF7GSE15244 193797844 193799281 1437 0
Stat6 IL-4-hr1GSE17850 193754141 193754712 571 0
TFAP2C MCF7GSE21234 193886303 193886641 338 0
hScc1 BcellGSE12603 193609790 193610186 396 0
hScc1 BcellGSE12603 193644657 193645330 673 0
hScc1 BcellGSE12603 193667865 193668116 251 0
hScc1 BcellGSE12603 193714787 193715042 255 0
hScc1 BcellGSE12603 193767011 193767652 641 0
hScc1 BcellGSE12603 193888238 193888816 578 0
hScc1 CdLSGSE12603 193644575 193645601 1026 0
hScc1 CdLSGSE12603 193667865 193668356 491 0
hScc1 CdLSGSE12603 193766870 193767689 819 0
hScc1 G2GSE9613 193609293 193610510 1217 0
hScc1 G2GSE9613 193644289 193645330 1041 0
hScc1 G2GSE9613 193667664 193668356 692 0
hScc1 G2GSE9613 193766833 193767652 819 0
hScc1 G2GSE9613 193771682 193772326 644 0
Validated miRNA targets Top
Cis-Nats regulation Top

Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018


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