AutismKB 2.0

Annotation Detail for MEGF11


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Basic Information Top
Gene Symbol:MEGF11 ( DKFZp434L121,KIAA1781 )
Gene Full Name: multiple EGF-like-domains 11
Band: 15q22.31
Quick LinksEntrez ID:84465; OMIM: 612454; Uniprot ID:MEG11_HUMAN; ENSEMBL ID: ENSG00000157890; HGNC ID: 29635
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
270N-linked (GlcNAc...) (Potential).
531N-linked (GlcNAc...) (Potential).
Location(AA) Modifications Resource
No data
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_032445
  • Location:chr15 63974692-64333128
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
Fos K562GSE19551 64349138 64349623 485 16252
H3K27me3 colorectalcancer 64335292 64336351 1059 2693
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CBP JurkatGSE17954 64232838 64234856 2018 0
CBP T0-glioblastomaGSE21026 64100385 64100604 219 0
CTCF CD4GSE12889 64270930 64271145 215 0
CTCF CD4SISSRdata 64270930 64271145 215 0
CTCF JurkatGSE12889 64270995 64271159 164 0
CTCF G2GSE9613 63994876 63995149 273 0
CTCF G2GSE9613 63996016 63996426 410 0
CTCF G2GSE9613 64042487 64042776 289 0
CTCF G2GSE9613 64061402 64062146 744 0
CTCF G2GSE9613 64077833 64078107 274 0
CTCF G2GSE9613 64100454 64100639 185 0
CTCF G2GSE9613 64139438 64139699 261 0
CTCF G2GSE9613 64160237 64160692 455 0
CTCF G2GSE9613 64183519 64183674 155 0
CTCF G2GSE9613 64188136 64188681 545 0
CTCF G2GSE9613 64195426 64195640 214 0
CTCF G2GSE9613 64213541 64213751 210 0
CTCF G2GSE9613 64228069 64228567 498 0
CTCF G2GSE9613 64235831 64236065 234 0
CTCF G2GSE9613 64239002 64239164 162 0
CTCF G2GSE9613 64259818 64259958 140 0
CTCF G2GSE9613 64280555 64281018 463 0
CTCF G2GSE9613 64307664 64308060 396 0
CTCF G2GSE9613 64311541 64311876 335 0
CTCF G2GSE9613 64331464 64332167 703 0
CTCF G2GSE9613 64332493 64332706 213 0
ER E2-MCF7GSE14664 64212608 64212643 35 0
ER Fulvestrant-MCF7GSE14664 64142024 64142124 100 0
FOXA1 MCF7GSE15244 64122468 64123179 711 0
FOXA1 eGFPGSE10845 64122468 64123179 711 0
Fos K562GSE19551 64099376 64099822 446 0
Gata1 K562GSE18868 64270800 64271241 441 0
H3K27me3 colorectalcancer 64330708 64331329 621 0
Myc hESGSE17917 64145231 64145588 357 0
NFkBII GM10847GSE19485 63995863 63997336 1473 0
NFkBII GM12878GSE19485 63995911 63998797 2886 0
NFkBII GM12892GSE19485 63995910 63998912 3002 0
NFkBII GM15510GSE19485 63995693 63997411 1718 0
NFkBII GM18526GSE19485 63995728 63997578 1850 0
NRSF JurkatGSE13047 64031403 64032955 1552 0
NRSF JurkatGSE13047 64082727 64085806 3079 0
NRSF mAbJurkat 64028221 64029533 1312 0
NRSF mAbJurkat 64030164 64030679 515 0
NRSF mAbJurkat 64031603 64032537 934 0
NRSF mAbJurkat 64032945 64034757 1812 0
NRSF mAbJurkat 64079951 64081855 1904 0
NRSF mAbJurkat 64082687 64083826 1139 0
NRSF mAbJurkat 64084272 64085209 937 0
NRSF mAbJurkat 64085547 64086834 1287 0
NRSF mAbJurkat 64087168 64087755 587 0
NRSF mAbJurkat 64088306 64088943 637 0
NRSF-mono JurkatQuESTdata 64031500 64033405 1905 0
NRSF-mono JurkatQuESTdata 64083537 64085805 2268 0
NRSF-poly JurkatQuESTdata 64031486 64033631 2145 0
NRSF-poly JurkatQuESTdata 64083956 64085081 1125 0
Nanog hESGSE18292 64184748 64185257 509 0
Oct1 H2O2-HelaGSE14283 64021548 64021575 27 0
Oct1 H2O2-HelaGSE14283 64204995 64205026 31 0
Oct1 H2O2-HelaGSE14283 64270468 64270505 37 0
Oct1 HelaGSE14283 63978327 63978358 31 0
Oct1 HelaGSE14283 64021542 64021579 37 0
Oct1 HelaGSE14283 64198639 64198709 70 0
Oct1 HelaGSE14283 64204995 64205026 31 0
Oct1 HelaGSE14283 64214428 64214460 32 0
Oct1 HelaGSE14283 64270468 64270521 53 0
Oct1 HelaGSE14283 64286334 64286365 31 0
Oct1 HelaGSE14283 64307082 64307115 33 0
Oct4 hESGSE17917 64146921 64147403 482 0
Oct4 hESGSE21916 64033548 64034380 832 0
Oct4 hESGSE21916 64146848 64147578 730 0
Oct4 hESGSE21916 64259962 64260496 534 0
P300 T0-glioblastomaGSE21026 64100388 64100604 216 0
P300 T30-glioblastomaGSE21026 64100046 64100831 785 0
P300 T30-glioblastomaGSE21026 64152069 64152988 919 0
P300 T30-glioblastomaGSE21026 64159979 64160781 802 0
RNAII Tamoxifen-MCF7GSE14664 64123945 64124033 88 0
Sox2 hESGSE18292 64146982 64147468 486 0
Sox2 hESGSE18292 64184745 64184979 234 0
TFAP2C MCF7GSE21234 63981718 63982351 633 0
TFAP2C MCF7GSE21234 63985742 63986233 491 0
TFAP2C MCF7GSE21234 64033699 64034235 536 0
TFAP2C MCF7GSE21234 64084011 64084510 499 0
TFAP2C MCF7GSE21234 64181182 64181660 478 0
hScc1 BcellGSE12603 63996094 63996534 440 0
hScc1 BcellGSE12603 64061318 64061933 615 0
hScc1 BcellGSE12603 64068845 64069085 240 0
hScc1 BcellGSE12603 64097713 64097856 143 0
hScc1 BcellGSE12603 64133428 64133961 533 0
hScc1 BcellGSE12603 64157683 64157973 290 0
hScc1 BcellGSE12603 64174139 64174423 284 0
hScc1 BcellGSE12603 64175660 64176223 563 0
hScc1 BcellGSE12603 64180475 64180763 288 0
hScc1 BcellGSE12603 64195426 64195568 142 0
hScc1 BcellGSE12603 64215620 64215954 334 0
hScc1 BcellGSE12603 64231190 64231572 382 0
hScc1 BcellGSE12603 64233526 64233718 192 0
hScc1 BcellGSE12603 64247473 64247807 334 0
hScc1 BcellGSE12603 64248503 64248710 207 0
hScc1 BcellGSE12603 64263797 64264642 845 0
hScc1 BcellGSE12603 64271000 64271145 145 0
hScc1 BcellGSE12603 64300523 64300835 312 0
hScc1 BcellGSE12603 64304403 64304876 473 0
hScc1 BcellGSE12603 64316029 64316385 356 0
hScc1 BcellGSE12603 64330815 64331033 218 0
hScc1 BcellGSE12603 64331402 64333108 1706 0
Validated miRNA targets Top
Cis-Nats regulation Top
Cluster ID Plue Type Plus Gene Name Plus Chromosome Plus Start Plus End Overlap Length Minus Type Minus Gene Name Minus Chromosome Minus Star Minus End Type
8965 EST chr15 64095935 64100396 4461 mRNA MEGF11 chr15 63974692 64333129 Non-exonic Bidirectional (NOB) pairs

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