AutismKB 2.0

Annotation Detail for IFT122


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Basic Information Top
Gene Symbol:IFT122 ( CED,SPG,WDR10,WDR10p,WDR140 )
Gene Full Name: intraflagellar transport 122 homolog (Chlamydomonas)
Band: 3q21.3-q22.1
Quick LinksEntrez ID:55764; OMIM: 606045; Uniprot ID:IF122_HUMAN; ENSEMBL ID: ENSG00000163913; HGNC ID: 13556
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
1021N6-acetyllysine.
Location(AA) Modifications Resource
Location(AA) Modification Resource
70Phosphoserine(CK2)HMM predict
185N-linkedHMM predict
225Phosphoserine(ATM)HMM predict
228Phosphoserine(CK2)HMM predict
241Phosphoserine(ATM)HMM predict
273Phosphothreonine(PKC)HMM predict
294Phosphotyrosine(INSR)HMM predict
316Phosphothreonine(PKC)HMM predict
335Phosphotyrosine(Syk)HMM predict
535N-linkedHMM predict
575Phosphotyrosine(INSR)HMM predict
575Phosphotyrosine(Jak)HMM predict
598N-linkedHMM predict
679Phosphoserine(CK2)HMM predict
865Phosphotyrosine(Syk)HMM predict
865Phosphotyrosine(INSR)HMM predict
916SulfotyrosineHMM predict
917SulfotyrosineHMM predict
1058S-palmitoylHMM predict
1104Phosphothreonine(CK2)HMM predict
1130N-linkedHMM predict
1131N-linkedHMM predict
1217PhosphoserineHMM predict
1220Phosphotyrosine(INSR)HMM predict
1229S-palmitoylHMM predict
1230S-palmitoylHMM predict
1233CysteineHMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_018262
  • Location:chr3 130641657-130721879
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
PHF8 293TGSE20725 130640931 130642360 1429 12
TFAP2C MCF7GSE21234 130641181 130642114 933 10
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
TFAP2C MCF7GSE21234 130722347 130722870 523 729
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CBP T30-glioblastomaGSE21026 130695884 130697116 1232 0
CTCF CD4GSE12889 130691678 130692064 386 0
CTCF CD4SISSRdata 130691678 130692064 386 0
CTCF HelaGSE12889 130691836 130692048 212 0
CTCF JurkatGSE12889 130691683 130692128 445 0
CTCF G2GSE9613 130641985 130642185 200 0
CTCF G2GSE9613 130683147 130683485 338 0
CTCF G2GSE9613 130684393 130684528 135 0
CTCF G2GSE9613 130689108 130689493 385 0
CTCF G2GSE9613 130691749 130692151 402 0
CTCF G2GSE9613 130702548 130702844 296 0
CTCF G2GSE9613 130714041 130714560 519 0
CTCF G2GSE9613 130715930 130716741 811 0
CTCF G2GSE9613 130717008 130717350 342 0
CTCF G2GSE9613 130718600 130720029 1429 0
ER E2-MCF7GSE14664 130695102 130695171 69 0
ER MCF7GSE19013 130686975 130687794 819 0
ER MCF7GSE19013 130700555 130701244 689 0
ER MCF7GSE19013 130707759 130708485 726 0
FOXA1 MCF7GSE15244 130686843 130690003 3160 0
FOXA1 MCF7GSE15244 130695176 130695401 225 0
FOXA1 MCF7GSE15244 130696042 130698441 2399 0
FOXA1 MCF7GSE15244 130699990 130702584 2594 0
FOXA1 MCF7GSE15244 130706616 130708862 2246 0
Fos K562GSE19551 130641330 130642087 757 0
FoxA1 MCF7MACSdata 130707962 130708285 323 0
H3K4me2 HCT116GSE10453 130642667 130642881 214 0
H3ac HepG2E 130642667 130642881 214 0
Myc K562GSE19551 130649610 130650231 621 0
Nanog hESGSE18292 130687907 130688336 429 0
Oct1 H2O2-HelaGSE14283 130680112 130680141 29 0
Oct1 H2O2-HelaGSE14283 130720692 130720721 29 0
Oct1 HelaGSE14283 130680112 130680141 29 0
Oct1 HelaGSE14283 130720692 130720720 28 0
P300 T0-glioblastomaGSE21026 130662843 130663581 738 0
P300 T0-glioblastomaGSE21026 130696207 130697099 892 0
P300 T30-glioblastomaGSE21026 130686672 130688255 1583 0
P300 T30-glioblastomaGSE21026 130695819 130697522 1703 0
PHF8 HeLaGSE20725 130640773 130642589 1816 0
PHF8 Hs68plusFBSGSE20725 130640785 130642574 1789 0
RARA MCF7GSE15244 130686843 130689394 2551 0
RARA MCF7GSE15244 130691712 130693052 1340 0
RARA MCF7GSE15244 130695895 130698441 2546 0
RARA MCF7GSE15244 130699990 130702584 2594 0
RARA MCF7GSE15244 130705021 130705587 566 0
RARA MCF7GSE15244 130706552 130708935 2383 0
RARG MCF7GSE15244 130686843 130689434 2591 0
RARG MCF7GSE15244 130691825 130693089 1264 0
RARG MCF7GSE15244 130694935 130695542 607 0
RARG MCF7GSE15244 130695895 130698441 2546 0
RARG MCF7GSE15244 130699914 130702922 3008 0
RARG MCF7GSE15244 130704707 130705661 954 0
RARG MCF7GSE15244 130706518 130709616 3098 0
Sox2 hESGSE18292 130687843 130688242 399 0
Stat6 IL-4-hr4GSE17850 130653492 130654020 528 0
TFAP2C MCF7GSE21234 130686670 130687877 1207 0
TFAP2C MCF7GSE21234 130707771 130708567 796 0
hScc1 BcellGSE12603 130691478 130693021 1543 0
hScc1 BcellGSE12603 130716037 130716352 315 0
hScc1 CdLSGSE12603 130691478 130692230 752 0
hScc1 G2GSE9613 130691749 130692151 402 0
hScc1 G2GSE9613 130718600 130719021 421 0
p130 QuiescentGSE19898 130697071 130697251 180 0
p130 SenescentGSE19898 130662627 130662985 358 0
p130 shRbSenescentGSE19898 130663128 130663476 348 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
18668 mRNA WDR10 chr3 130641665 130721888 55 EST chr3 130639358 130641720Sense/Antisense (SA) 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


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