AutismKB 2.0

Annotation Detail for CEP152


View Evidences View Variants View Annotations
Basic Information Top
Gene Symbol:CEP152 ( FLJ21594,KIAA0912 )
Gene Full Name: centrosomal protein 152kDa
Band: 15q21.1
Quick LinksEntrez ID:22995; OMIM: 613529; Uniprot ID:CE152_HUMAN; ENSEMBL ID: ENSG00000103995; HGNC ID: 29298
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
Location(AA) Modification
1258Phosphotyrosine.
1405Phosphoserine.
Location(AA) Modifications Resource
Location(AA) Modification Resource
19Phosphotyrosine(INSR)HMM predict
19SulfotyrosineHMM predict
19Phosphotyrosine(Syk)HMM predict
24Phosphotyrosine(INSR)HMM predict
24Phosphotyrosine(Syk)HMM predict
24SulfotyrosineHMM predict
47Phosphoserine(CK1)HMM predict
48Phosphoserine(MAPK)HMM predict
83Phosphoserine(ATM)HMM predict
85Phosphoserine(IKK)HMM predict
112N-linkedHMM predict
114Phosphoserine(CDC2)HMM predict
167N-linkedHMM predict
197Phosphoserine(ATM)HMM predict
337Phosphoserine(ATM)HMM predict
389Phosphoserine(CK1)HMM predict
404Phosphoserine(CK1)HMM predict
432Phosphothreonine(PKA)HMM predict
507Phosphoserine(CK2)HMM predict
585Phosphotyrosine(Abl)HMM predict
664Phosphothreonine(PKC)HMM predict
695Phosphothreonine(PKA)HMM predict
700Phosphoserine(CK1)HMM predict
700Phosphoserine(IKK)HMM predict
757N-linkedHMM predict
886SulfotyrosineHMM predict
886Phosphotyrosine(EGFR)HMM predict
947SulfotyrosineHMM predict
970Phosphoserine(ATM)HMM predict
970Phosphoserine(CK2)HMM predict
970Phosphoserine(CK2)HMM predict
1034Phosphoserine(ATM)HMM predict
1075S-palmitoylHMM predict
1100S-palmitoylHMM predict
1148Phosphothreonine(CDK)HMM predict
1148Phosphothreonine(MAPK)HMM predict
1214Phosphothreonine(PKC)HMM predict
1251Phosphothreonine(PKC)HMM predict
1264Phosphoserine(ATM)HMM predict
1264Phosphoserine(IKK)HMM predict
1266Phosphoserine(CK1)HMM predict
1266Phosphoserine(IKK)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_014985
  • Location:chr15 46817639-46890475
  • strand:-
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 46891151 46891376 225 788
E2F4 G0GSE7516 46889845 46891228 1383 61
E2F4 SGSE7516 46890248 46891044 796 171
ETS1 JurkatGSE17954 46890076 46891071 995 98
Fos K562GSE19551 46890282 46891038 756 185
LIN54 G0GSE7516 46890320 46891080 760 225
LIN9 G0GSE7516 46889924 46891579 1655 276
LIN9 SGSE7516 46890028 46891579 1551 328
Rb GrowingGSE19898 46890634 46890854 220 269
Rb QuiescentGSE19898 46890540 46890969 429 279
Rb SenescentGSE19898 46890585 46890947 362 291
Rb shRbSenescenceGSE19898 46890589 46890886 297 262
hScc1 BcellGSE12603 46890455 46890867 412 186
p130 QuiescentGSE19898 46890378 46891009 631 218
p130 SenescentGSE19898 46890274 46891007 733 165
p130 shRbQuiescentGSE19898 46890013 46891030 1017 46
p130 shRbSenescentGSE19898 46890426 46891090 664 283
p130 G0GSE7516 46890028 46891186 1158 132
p130 SGSE7516 46890028 46890971 943 24
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
P300 T30-glioblastomaGSE21026 46802431 46803223 792 14813
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
H3K4me3 colorectalcancer 46889316 46890610 1294 0
Nanog ESGSE20650 46877808 46878152 344 0
P300 T30-glioblastomaGSE21026 46889527 46891061 1534 0
PAX3-FKHR Rh4GSE19063 46876075 46877043 968 0
TAF HelaGSE8489 46889735 46890645 910 0
TFAP2C MCF7GSE21234 46889932 46890422 490 0
hScc1 BcellGSE12603 46874231 46874533 302 0
p63 keratinocytesGSE17611 46839128 46839987 859 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
8797 mRNA chr15 46890200 46891397 70 mRNA Cep152 chr15 46820636 46890519Sense/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