AutismKB 2.0

Annotation Detail for C14orf79


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Basic Information Top
Gene Symbol:C14orf79 ( - )
Gene Full Name: chromosome 14 open reading frame 79
Band: 14q32.33
Quick LinksEntrez ID:122616; OMIM: NA; Uniprot ID:CN079_HUMAN; ENSEMBL ID: ENSG00000140104; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
32Phosphoserine(CK1)HMM predict
35Phosphoserine(CK1)HMM predict
87Phosphoserine(PKA)HMM predict
113O-linkedHMM predict
114Phosphoserine(PKB)HMM predict
140O-linkedHMM predict
205O-linkedHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_174891
  • Location:chr14 104523660-104532899
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CBP T30-glioblastomaGSE21026 104510311 104511050 739 12980
CTCF CD4GSE12889 104513533 104513907 374 9941
CTCF CD4SISSRdata 104513533 104513907 374 9941
CTCF JurkatGSE12889 104513533 104513839 306 9975
CTCF G2GSE9613 104503563 104504166 603 19796
CTCF G2GSE9613 104505044 104505673 629 18302
CTCF G2GSE9613 104506143 104506869 726 17155
CTCF G2GSE9613 104507456 104508462 1006 15702
CTCF G2GSE9613 104508964 104509354 390 14502
CTCF G2GSE9613 104509752 104510687 935 13441
CTCF G2GSE9613 104512778 104515772 2994 9386
CTCF G2GSE9613 104516710 104517097 387 6757
CTCF G2GSE9613 104517471 104518778 1307 5536
CTCF G2GSE9613 104519750 104520168 418 3702
CTCF G2GSE9613 104521534 104521938 404 1925
CTCF G2GSE9613 104522951 104523835 884 268
Fos K562GSE19551 104515702 104516032 330 7794
FoxA1 MCF7MACSdata 104509631 104509809 178 13941
P300 T30-glioblastomaGSE21026 104510372 104511331 959 12809
PHF8 Hs68plusFBSGSE20725 104522784 104523810 1026 364
RARG MCF7GSE15244 104517471 104517909 438 5971
TFAP2C MCF7GSE21234 104505384 104506937 1553 17500
TFAP2C MCF7GSE21234 104509473 104511314 1841 13267
hScc1 BcellGSE12603 104503419 104504106 687 19898
hScc1 BcellGSE12603 104504934 104505372 438 18508
hScc1 BcellGSE12603 104506253 104506869 616 17100
hScc1 BcellGSE12603 104507755 104508104 349 15731
hScc1 BcellGSE12603 104509713 104510108 395 13750
hScc1 BcellGSE12603 104512956 104514372 1416 9997
hScc1 BcellGSE12603 104515123 104515869 746 8165
hScc1 BcellGSE12603 104518624 104519678 1054 4510
hScc1 BcellGSE12603 104523355 104523835 480 66
hScc1 CdLSGSE12603 104506499 104506895 396 16964
hScc1 CdLSGSE12603 104513121 104514142 1021 10029
hScc1 CdLSGSE12603 104515157 104515772 615 8196
p130 QuiescentGSE19898 104510967 104511221 254 12567
p130 shRbQuiescentGSE19898 104504655 104505188 533 18739
p130 shRbQuiescentGSE19898 104509968 104510416 448 13469
p130 shRbQuiescentGSE19898 104510752 104511190 438 12690
p130 shRbQuiescentGSE19898 104511560 104511969 409 11896
p130 shRbSenescentGSE19898 104523276 104523561 285 242
p63 keratinocytesGSE17611 104519912 104520727 815 3341
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 104527374 104527567 193 0
CTCF G2GSE9613 104528942 104529253 311 0
CTCF G2GSE9613 104530583 104530881 298 0
p130 shRbQuiescentGSE19898 104523646 104524070 424 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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